Implanet Announces Its Half-Yearly Report on the Liquidity Contract With ODDO Corporate Finance

July 07, 2017

BORDEAUX, France & BOSTON–(BUSINESS WIRE)–Regulatory News:

Pursuant to the liquidity contract entrusted to ODDO Corporate Finance by IMPLANET (Paris:IMPL) (OTCQX:IMPZY) (Euronext: IMPL, FR0010458729, PEA-PME eligible), on 30 June 2017 the following assets appeared on the liquidity account:

  • Number of shares: 134,950
  • Cash balance of the liquidity account: €46,060.29

As a reminder, at the time of the last half-yearly report on 31 December 2016, the following resources were booked to the liquidity account:

  • Number of shares: 136,500
  • Cash balance of the liquidity account: €40,003.79

As a reminder, at the time of the settlement of the contract, the following resources were booked to the liquidity account:

  • Number of shares: 0
  • Cash balance of the liquidity account: €400,000.00

About IMPLANET
Founded in 2007, IMPLANET is a medical technology company that manufactures high-quality implants for orthopedic surgery. Its flagship product, the JAZZ latest-generation implant, aims to treat spinal pathologies requiring vertebral fusion surgery. Protected by four families of international patents, JAZZ has obtained 510(k) regulatory clearance from the Food and Drug Administration (FDA) in the United States and the CE mark. IMPLANET employs 48 staff and recorded 2016 sales of €7.8 million. For further information, please visit www.implanet.com.
Based near Bordeaux in France, IMPLANET established a US subsidiary in Boston in 2013.
IMPLANET is listed on Compartment C of the Euronext™ regulated market in Paris.

Contacts

IMPLANET
Ludovic Lastennet
CEO
Tel. : +33 (0)5 57 99 55 55
investors@implanet.com
or
NewCap
Investor Relations
Florent Alba, Tel. : +33 (0)1 44 71 94 94
implanet@newcap.eu
or
NewCap
Media Relations
Nicolas Merigeau, Tel. : +33 (0)1 44 71 94 98
implanet@newcap.eu
or
AlphaBronze
US-Investor Relations
Pascal Nigen, Tel.: +1 917 385 21 60
implanet@alphabronze.net

SpineGuard posts 16% growth for H1 2017, appoints co-Founder Stéphane Bette as CEO

July 06, 2017

PARIS & SAN FRANCISCO–(BUSINESS WIRE)–Regulatory News:

SpineGuard (FR0011464452)(Paris:ALSGD), an innovative company that develops and markets disposable medical devices designed to make spine surgery safer, announced:

  • First-half global revenue growth of 16% (13% cc) to €4.2M, compared with €3.6M in the first half of 2016;
  • The appointment of Stéphane Bette, co-Founder, CTO and US General Manager, as CEO of the company effective on July 13th; Pierre Jérôme, who has served as CEO since the company’s founding, will continue to serve as Board Director of the company;
  • The implementation of a profitability plan to reach monthly breakeven by the end of 2018.

H1 and Q2 2017 revenues

€ thousands – IFRS 2017 2016 Variance
First Quarter 2,169 1,760 +23%
Second Quarter 2,030 1,873 +8%
Half-Year 4,199 3,633 +16%

Unaudited

Global revenue in the second quarter of 2017 increased 8% on a reported basis and 6% at constant exchange rate (cc). In the first half, global revenue increased 16% (13% cc) to €4,199k, compared with €3,633k in the first half of 2016.

In the first half of 2017, 4,264 DSG units were sold compared with 4,351 in the first half of 2016, including 2,589 (61%) in the United States, where revenue grew 19% (15% cc) to €3,397k in the first half of 2017 compared with €2,866k in the same period last year.

Appointment of Stéphane Bette, Co-founder, as CEO

The Board of Directors has appointed Stéphane Bette, its US General Manager, CTO and co-Founder, as CEO of SpineGuard SA in succession of Pierre Jérôme, who continues to serve as a Board Director of the company.

Stéphane brings more than 20 years of experience in the spinal industry to the role. He co-founded the company and has led the US operations since 2009 while also retaining his role as Chief Technology Officer during this period. Prior to this, Stéphane spent 10 years at SpineVision, a private spine company, in a number of roles, ending as US General Manager. He started his career at Sofamor Danek in the 1990’s, prior to its acquisition by Medtronic. Stéphane received a Master’s degree in Mechanical Engineering from ENSAM, France, and a Postgraduate Degree in Biomechanics from LBM in Paris, France.

“The Board is very pleased to appoint Stéphane as CEO to lead the company through its next stage of growth,” said Alan Olsen, Chairman. “He has led the company’s increasingly important US operations since 2009 as well as overseen the development of SpineGuard’s core DSG™ technology platform. He is a natural successor to his co-Founder Pierre Jérôme, whom we warmly thank for his leadership of the company over the past 8 years. Under Pierre’s stewardship, SpineGuard has grown from a one-product company with €1 million in sales, through multiple fund-raising rounds, including an IPO in 2013, to the strong position it is in today. We are very pleased to have Pierre continue his association with the company in his role as Director with a particular focus on strategic and business development initiatives.

“SpineGuard is a high-performing company with a cohesive team and a unique technology in DSG™”, Stéphane Bette commented. “We delivered double-digit growth this first half of the year in a context where we are preparing for the US launch of our smart DSG™ screw. I look forward to intensifying SpineGuard’s focus on leveraging our core DSG™ platform through additional deals in spine and other musculoskeletal segments while continuing to grow our organic sales, capitalizing on our strong commercial, marketing and clinical foundations and rebalancing the organization. In order to reach financial freedom, we have set a specific goal that SpineGuard reaches breakeven by the end of 2018 and then profitability.”

Pierre Jérôme concluded: “After driving SpineGuard with close support from Stéphane since its inception, I am particularly glad to hand over the baton to him now – when momentum is building for the company with sustained growth, promising perspectives in China and the further deployment of our DSG™ technology platform in spine and dental through our partnership strategy. This smooth transition will provide continuity for our employees, customers and partners.”

Business focus for 2017 and 2018

To reach breakeven by the end of 2018, SpineGuard will concentrate its efforts on:

  • Signing new industry partnerships for expanded commercial applications of its proprietary digital DSG™ technology within the spinal and broader musculoskeletal sector to trigger new sources of revenue;
  • Growing its worldwide sales with a primary commercial focus on the US market which accounts for close to 80% of revenues;
  • Implementing a profitability plan to right size its organization, capitalizing on its strengths and leveraging its cutting-edge proprietary DSG™ platform.

Next financial press release: 2017 Half-year financial results on September 14, 2017

About SpineGuard®

Founded in 2009 in France and the USA, by Pierre Jérôme and Stéphane Bette, SpineGuard’s mission is to make spine surgery safer by bringing real-time digital technology into the operating room. Its primary objective is to establish its proprietary DSG™ (Dynamic Surgical Guidance) technology as the global standard of surgical care, starting with safer screw placement in spine surgery and then in other surgeries. PediGuard®, the first device designed using DSG, was co-invented by Maurice Bourlion, Ph.D., Ciaran Bolger, M.D., Ph.D., and Alain Vanquaethem, Biomedical Engineer. It is the world’s first and only handheld device capable of alerting surgeons to potential pedicular or vertebral breaches. Over 50,000 surgical procedures have been performed worldwide with DSG™ enabled devices. Numerous studies published in peer-reviewed medical and scientific journals have demonstrated the multiple benefits that PediGuard® delivers to patients, surgical staff and hospitals. SpineGuard is expanding the scope of its DSG™ platform through strategic partnerships with innovative medical device companies and the development of smart instruments and implants. SpineGuard has offices in San Francisco and Paris. For further information, visit www.spineguard.com.

Disclaimer

The SpineGuard securities may not be offered or sold in the United States as they have not been and will not be registered under the Securities Act or any United States state securities laws, and SpineGuard does not intend to make a public offer of its securities in the United States. This is an announcement and not a prospectus, and the information contained herein does and shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of the securities referred to herein in the United States in which such offer, solicitation or sale would be unlawful prior to registration or exemption from registration.

Contacts

SpineGuard
Manuel Lanfossi, +33 (0)1-4518-4519
Chief Financial Officer
m.lanfossi@spineguard.com
or
Europe / NewCap
Investor Relations & Financial Communication
Florent Alba / Pierre Laurent
+33 (0)1-44-7194-94
spineguard@newcap.fr
or
US
Ronald Trahan Associates Inc.
Ronald Trahan, APR
+1-508-359-4005, x108

NuVasive Announces Conference Call And Webcast Of Second Quarter 2017 Results

SAN DIEGOJuly 5, 2017 /PRNewswire/ — NuVasive, Inc. (NASDAQ: NUVA), a leading medical device company focused on transforming spine surgery with minimally disruptive, procedurally-integrated solutions, today announced the Company will release its second quarter 2017 earnings results on Thursday, July 27, 2017 after the close of the market.

NuVasive will hold a conference call on Thursday, July 27, 2017 at 4:30 p.m. ET / 1:30 p.m. PT to discuss the results of its financial performance for the second quarter 2017. The dial-in numbers are 1-877-407-9039 for domestic callers and 1-201-689-8470 for international callers. A live webcast of the conference call will be available online from the Investor Relations page of the Company’s website at www.nuvasive.com.

After the live webcast, the call will remain available on NuVasive’s website through August 28, 2017. In addition, a telephone replay of the call will be available until August 3, 2017. The replay dial-in numbers are 1-844-512-2921 for domestic callers and 1-412-317-6671 for international callers. Please use pin number: 13665648.

About NuVasive

NuVasive, Inc. (NASDAQ: NUVA) is transforming spine surgery and beyond with minimally invasive, procedurally-integrated solutions designed to deliver reproducible and clinically-proven surgical outcomes. The Company’s portfolio includes access instruments, implantable hardware, biologics, software systems for surgical planning, navigation and imaging solutions, magnetically adjustable implant systems for spine and orthopedics, and intraoperative monitoring service offerings. With $962 million in revenues (2016), NuVasive has an approximate 2,300 person workforce in more than 40 countries serving surgeons, hospitals and patients. For more information, please visit www.nuvasive.com.

Forward-Looking Statements

NuVasive cautions you that statements included in this news release that are not a description of historical facts are forward-looking statements that involve risks, uncertainties, assumptions and other factors which, if they do not materialize or prove correct, could cause NuVasive’s results to differ materially from historical results or those expressed or implied by such forward-looking statements. The potential risks and uncertainties which contribute to the uncertain nature of these statements include, but are not limited to, the risk that NuVasive’s revenue or earnings projections may turn out to be inaccurate because of the preliminary nature of the forecasts; the risk of further adjustment to financial results or future financial expectations; unanticipated difficulty in selling products, generating revenue or producing expected profitability; and those  other risks and uncertainties more fully described in NuVasive’s news releases and periodic filings with the Securities and Exchange Commission. NuVasive’s public filings with the Securities and Exchange Commission are available at www.sec.gov. NuVasive assumes no obligation to update any forward-looking statement to reflect events or circumstances arising after the date on which it was made.

SOURCE NuVasive, Inc.

Is Mazor Robotics Really on Track for Its Best Quarter Ever?

 – July 6, 2017

Mazor Robotics Ltd. (NASDAQ: MZOR) saw its shares make a handy gain on Thursday after the Israeli firm announced that it’s projecting it will report record revenues for the second quarter. It didn’t stop here. Mazor also said that it received a total of 19 purchase orders during the quarter as well, setting up for what could be its strongest quarter ever.

Currently the firm is expecting to see roughly $15.4 million in revenue for the second quarter, which compares to $8.3 million in the same period of last year. Obviously that’s incredible growth, but what do the analysts have to say?

Thomson Reuters consensus estimates are calling for only $12.36 million in this quarter, so Mazor might see a pretty solid beat. Even the highest revenue target among the six analysts covering Mazor is $13.45 million.

Looking at the bottom line, the firm didn’t give out any predictions, but the consensus estimate is $0.19 in earnings per share (EPS), versus last year’s $0.18 in EPS. Considering the ramp up in purchase orders, we might see this number come up in the weeks ahead of the report.

 

READ THE REST HERE

Zimmer Biomet Holdings Announces Live Audio Webcast and Conference Call of Second Quarter 2017 Results

WARSAW, Ind., June 30, 2017 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH) today announced its second quarter sales and earnings conference call will be broadcast live over the Internet on Thursday, July 27, 2017, at 8 a.m. Eastern Time.  A news release detailing the quarterly results will be made available at 7:30 a.m. Eastern Time the morning of the conference call.

The live audio webcast can be accessed via Zimmer Biomet’s Investor Relations website at http://investor.zimmerbiomet.com. It will be archived for replay following the conference call.

Individuals in the U.S. and Canada who wish to dial into the conference call may do so by dialing (888) 312-9837 and entering conference ID 7278985.  For a complete listing of international toll-free and local numbers, please visit http://investor.zimmerbiomet.com.  A digital recording will be available 24 hours after the completion of the conference call, from July 28, 2017 to August 26, 2017.  To access the recording, U.S. callers should dial (888) 203-1112 and international callers should dial +1 (719) 457-0820, and enter the Access Code ID 7278985.

About the Company

Founded in 1927 and headquartered in Warsaw, Indiana, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; office based technologies; spine, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

We have operations in more than 25 countries around the world and sell products in more than 100 countries. For more information, visit www.zimmerbiomet.com, or follow Zimmer Biomet on Twitter at www.twitter.com/zimmerbiomet.

ZBH – Fin

SOURCE Zimmer Biomet Holdings, Inc.

Related Links

http://www.zimmer.com

Bonesupport closes $57m IPO

BY

BoneSupport said last week it closed its initial public offering, raising a total of approximately $57.1 million (SEK 500 million), not including an over-allotment option.

The Swedish company, which is developing the Cerament G injectable antibiotic-eluting bone graft substitute, said it floated approximately 17.2 million new shares at $3.40 per share (SEK 29) in the round, raising approximately $57.1 million before issue costs and $54 million (SEK 461 million) after issue costs.

Bonesupport also issued an over-allotment option for 2.6 million shares and an additional $8.7 million (SEK 75 million), bringing the total number of shares offered in the round to 48.8 million, according to a press release.

 

READ THE REST HERE

Intellirod Spine™ Acquires New IP

AKRON, Ohio, June 28, 2017 (GLOBE NEWSWIRE) — Intellirod Spine, the spinal implant company developing disposable and implantable wireless RFID sensor technology for monitoring spinal rod strains, secured additional equity financing from new and existing investors led by the OhioHealth Innovation Development Fund and Queen City Angel First Fund V.  Funds will be used to reach key milestones toward the commercialization of the company’s sensor technologies and related lumbar fusion implants.

Intellirod Spine recently had the first human use of LOADPRO™ in an approved clinical study at Norton Leatherman Spine Center by Dr. Jeffrey Gum.  The company’s intraoperative LOADPRO™ sensor was used to record strains on spinal rods during a kyphotic deformity correction surgery.  Dr. Gum says, “We are very excited about the start of the clinical trial. Although the data was blinded to us intraoperatively, the post-hoc review shows promising results.  This exciting technology will provide valuable information that will help guide intraoperative decision making and potentially lead to non-invasive or non-ionizing information to help assess construct stability and fusion status.  We look forward to the progress of the study”.  This is meant to help surgeons quantify their tactile feel of the forces being applied during the deformity correction.   The company is pursuing a de novo 510(k) at the FDA and is simultaneously seeking a CE Mark for LOADPRO™.  According to Ric Navarro, Intellirod CEO, “This new information will not only help the surgeon but will help us with our FDA and CE Mark approvals”.  Two additional clinical sites include Grant Medical Center in Columbus, Ohio and the Cleveland Clinic in Cleveland, Ohio.  The company is also actively seeking a fourth site.

The company is announcing its entrance into the Digital Health space with new intellectual property paving the way toward in-home remote monitoring through its IntelliBrace™ project.  They anticipate being the first to offer autonomous data collection from their wireless implant, the ACCUVISTA™ rod strain sensor.  This will position the company to provide caregivers more information about the state of the implant and other measured parameters aimed at improving patient compliance and decreasing mobility related complications.  Dr. Chris Karas, a neurosurgeon at OhioHealth and inventor of the IntelliBrace™ concept, says, “Intellirod is focused on collecting the data surgeons need to achieve better outcomes for our patients.  This type of technology is currently lacking, but is absolutely necessary to get people back to work and back to life”.

The OhioHealth Innovation Development fund, which contributed to this project, supports physicians, nurses and associates working to bring their product ideas to life, while also giving them the opportunity to retain ownership of their intellectual property. “Dr. Karas, as an inventor of the IntelliBrace™, is a perfect example of how this OhioHealth fund can work. We are hoping this success story will encourage other brilliant, inventive minds at OhioHealth to dream big, and see those dreams turn into reality with funding help,” said Alan Nelson, OhioHealth Treasury Vice President.

Mr. Navarro stated the company is excited to make this evolution with its platform technology into the lower cost of care environment of the home to aid in the patient’s rehabilitation.  “Not only does IntelliBrace™ add new functional benefits but it will create cloud database opportunities for aggregating and interpreting data toward new norms in remote spine patient care”, says Mr. Navarro.

Intellirod has also signed a license agreement with the Cleveland Clinic to take its microelectronics and sensing know-how and technology into other parts of the spine with a therapeutic device with an integrated sensor.  The company is leveraging its platform of inductive powering and wireless communication into a therapeutic device to create a next generation “Smart” implant.  Cleveland Clinic’s Dr. Michael Steinmetz, who is a paid member of Intellirod’s scientific advisory board, says, “The LOADPRO System will provide data for enhancing surgical techniques and reducing complications and costs.  By sensing the progress of fusion through a sensor-enabled device we commonly use in spine fusions, our goal is to improve post-operative care.”

About Intellirod Spine
Intellirod Spine™ (formerly OrthoData Inc.) based in Akron, Ohio was founded by renowned spine surgeon Rolando M. Puno, M.D. and professors from the University of Louisville. The company is developing a wireless microelectronic spinal rod strain sensor and inductive power platform. This innovative strain monitoring system will allow spine surgeons to objectively assess the strain on spinal rods intraoperatively and postoperatively. www.intellirodspine.com

About Queen City Angels
The Queen City Angels (QCA) is a group of more than 50 experienced accredited investors who provide funding, support and guidance to early-stage growth companies in the Cincinnati area and surrounding region. QCA members, which include former C-level executives and entrepreneurs, draw from their personal operating and management experience to evaluate opportunities and provide on-going mentoring to young businesses with exceptional growth potential. Since 2000, QCA members have directly invested approximately $50 million in nearly 80 portfolio companies. The total capital invested in these companies, including QCA members’ capital, syndication partners’ capital, follow-on venture capital funds and venture debt is in excess of $410,000,000. CB Insight recently ranked QCA second out of 370 national angel organizations. For additional information, visit www.qca.com

About OhioHealth
OhioHealth is a nationally recognized, not-for-profit, charitable, healthcare outreach of the United Methodist Church.

Based in Columbus, Ohio, OhioHealth has been recognized as one of the top five large health systems in America by Truven Health Analytics, an honor it has received six times. It is also recognized by FORTUNE Magazine as one of the “100 Best Companies to Work For” and has been for 10 years in a row, 2007-2016.

Serving its communities since 1891, it is a family of 28,000 associates, physicians and volunteers, and a network of 11 hospitals, 50+ ambulatory sites, hospice, home-health, medical equipment and other health services spanning a 47-county area.

OhioHealth hospitals include OhioHealth Riverside Methodist Hospital, OhioHealth Grant Medical Center, OhioHealth Doctors Hospital, OhioHealth Grady Memorial Hospital, OhioHealth Dublin Methodist Hospital, OhioHealth Hardin Memorial Hospital, OhioHealth Marion General Hospital, OhioHealth O’Bleness Hospital, OhioHealth Mansfield Hospital, OhioHealth Shelby Hospital and OhioHealth Rehabilitation Hospital.

For more information, please visit our website at www.ohiohealth.com.

Contact Information:
Jennifer Dietrich, Intellirod Spine
phone: 234-678-8965 / email: jdietrich@intellirodspine.com
www.intellirodspine.com

As hospitals’ revenues shift from inpatient to outpatient setting, Saince’s new tool improves documentation quality

ALPHARETTA, Ga., June 27, 2017 /PRNewswire/ — Saince today announced the launch of PracticePerfect the much-awaited outpatient clinical documentation improvement (CDI) solution. PracticePerfect is the industry first and most comprehensive ambulatory CDI solution that includes tools for documentation improvement, risk adjustment and quality measures.

Hospitals are experiencing decreasing inpatient revenues and increasing outpatient volumes. A trend which has been continuing for the past several years. With the focus gradually shifting from inpatient to outpatient revenues, clinical documentation improvement in the outpatient setting is coming on to the center stage. At the same time, private and public insurance companies are paying increasing attention to physicians’ and hospitals’ quality scores.

PracticePerfect has the ability to automatically identify CMS and HHS Hierarchical Condition Categories (HCC) based on clinical codes, patient demographics, and other relevant criteria. Along with HCCs, the software also identifies prescription HCCs (RxHCC) and risk adjustment for End Stage Renal Disease (ESRD).

PracticePerfect also has inbuilt intelligence to identify pertinent quality measures and bring them to the attention of the physician at the point of care. This workflow will significantly improve the documentation quality at the physician level and their quality scores.

With integrated Group Practice Reporting Option (GPRO) quality measures as well, PracticePerfect will help Accountable Care Organizations (ACOs) participating in Shared Services Program in improving the quality of care they provide to their patient population.

Raghu Vir, President of Saince said, “A clinical documentation improvement tool like PracticePerfect is ideally suited to meet these evolving challenges of the healthcare industry. PracticePerfect is designed to help providers improve their clinical documentation standards, protect their reimbursements and monitor the quality of care they provide.”

The tool has attracted quite a bit of attention among healthcare providers and major hospital systems.

About Saince: Saince is a 15-year-old, award winning clinical documentation solutions and services company based in Atlanta, Ga. Saince is well recognized for its innovative solutions that help healthcare providers navigate and thrive in the fast changing healthcare industry landscape. Saince helps hospitals of all sizes and specialties – from critical access hospitals to large health systems- in saving costs, improving reimbursements and enhancing quality of care.

 

SOURCE Saince, Inc.

Related Links

http://www.saince.com

Nasdaq Stockholm Welcomes Bonesupport to the Main Market

Stockholm, June 21, 2017 — Nasdaq (Nasdaq: NDAQ) announced that Bonesupport Holding AB (short name: BONEX), a small cap company within the health care sector, has started trading of its shares on the main market of Nasdaq Stockholm. Bonesupport is the 63rd company to list at Nasdaq’s Nordic markets* in 2017.

Bonesupport is a Swedish commercial stage orthobiologics company aiming to improve the lives of patients suffering from bone disorders. The company develops and commercializes injectable bioceramic bone graft substitutes to treat bone voids, based on its novel, proprietary Cerament technology platform. Bonesupport is headquartered at the Ideon Science Park in Lund, Sweden, with additional sales offices in Germany and the US. For more information, please visit www.bonesupport.com.

“We are pleased to have completed our IPO on the Nasdaq Stockholm main market and that our shares have started trading today,” said Richard Davies, CEO of Bonesupport. “Our listing is a key step in supporting Bonesupport’s growth strategy. Our IPO has provided us with the funds to drive our sales in both the US and Europe, to generate additional clinical data to enhance the competitive positioning of our products, to complete the Fortify study, which is key to gaining US approval for Cerament G, and to invest in our pipeline. This strategy will allow us to deliver our 2020 financial targets and to generate significant value for shareholders.”

“We welcome Bonesupport to the Nasdaq Stockholm main market,” said Adam Kostyál, SVP and Head of European listings at Nasdaq. “We continue to see a strong inflow of health care sector companies leveraging the public markets as a platform for future growth, and Bonesupport will make an exciting addition to that list.”

*Main markets and Nasdaq First North at Nasdaq Copenhagen, Nasdaq Helsinki, Nasdaq Iceland and Nasdaq Stockholm.
About Nasdaq

Nasdaq (Nasdaq: NDAQ) is a leading global provider of trading, clearing, exchange technology, listing, information and public company services. Through its diverse portfolio of solutions, Nasdaq enables customers to plan, optimize and execute their business vision with confidence, using proven technologies that provide transparency and insight for navigating today’s global capital markets. As the creator of the world’s first electronic stock market, its technology powers more than 89 marketplaces in 50 countries, and 1 in 10 of the world’s securities transactions. Nasdaq is home to 3,800 total listings with a market value of $11 trillion. To learn more, visit: http://business.nasdaq.com

Nasdaq Copenhagen, Nasdaq Helsinki, Nasdaq Iceland, Nasdaq Riga, Nasdaq Stockholm, Nasdaq Tallinn, Nasdaq Vilnius, Nasdaq Clearing and Nasdaq Broker Services are respectively brand names for the regulated markets of Nasdaq Copenhagen A/S, Nasdaq Helsinki Ltd., Nasdaq Iceland hf., Nasdaq Riga, AS, Nasdaq Stockholm AB, Nasdaq Tallinn AS, AB Nasdaq Vilnius, Nasdaq Clearing AB and Nasdaq Broker Services AB. Nasdaq Nordic represents the common offering by Nasdaq Copenhagen, Nasdaq Helsinki, Nasdaq Iceland and Nasdaq Stockholm. Nasdaq Baltic represents the common offering by Nasdaq Tallinn, Nasdaq Riga and Nasdaq Vilnius.

Cautionary Note Regarding Forward-Looking Statements

The matters described herein contain forward-looking statements that are made under the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements include, but are not limited to, statements about Nasdaq and its products and offerings. We caution that these statements are not guarantees of future performance. Actual results may differ materially from those expressed or implied in the forward-looking statements. Forward-looking statements involve a number of risks, uncertainties or other factors beyond Nasdaq’s control. These factors include, but are not limited to factors detailed in Nasdaq’s annual report on Form 10-K, and periodic reports filed with the U.S. Securities and Exchange Commission. We undertake no obligation to release any revisions to any forward-looking statements.

Media Relations Contact:
Erik Granström
+46 73 449 78 07
erik.granstrom@nasdaq.com

Medicrea Announces Capital Raise of € 13 Million Through a Successful Private Placement

June 19, 2017

LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (ISIN : FR0004178572 – ALMED, eligible to PEA-PME), pioneering the convergence of healthcare IT and next-generation, outcome-centered device design and manufacturing with UNiD™ ASI technology, announced today the successful capital increase for the benefit of a specific category of beneficiaries through the accelerated construction of an order book.

Due to strong investor demand, the Company issued 2,680,413 new shares with a nominal value of € 0.16 per unit, at a unit price of € 4.85, including issue premium, for a total amount of € 13 million, compared to approximately € 10 million originally planned, representing 21.08% of the Company’s share capital after the transaction (the ‘Action’).

As an indication, the participation of a shareholder holding 1% of the share capital of the Company prior to the issue will become 0.79%.

The funds will be raised from international funds and / or investment companies carrying out multinational financial transactions in several, in support of Medicrea’s efforts:

1 / To accelerate the development, mainly in the United States, of the UNiD™ ASI platform to enable the Company to strengthen its position as a pioneer and world leader in personalized spinal technology, which includes comprehensive analytical services and biomechanical expertise for the collection and modeling of clinical data and the realization of patient-specific spinal implants; and

2 / To prepare for the commercialization of a new range of 3D-printed titanium interbody cages in the United States and Europe in preparation of pending regulatory clearances and sales agreements.

The proceeds of the capital increase associated with the current liquidity available should enable the Company to meet its future financial commitments over the next 18 months.

The Action was implemented by decision of the Board of Directors on 15 June, 2017 and the Chairman and Chief Executive Officer on 16 June, 2017, pursuant to the 9th Resolution approved by of the Combined Shareholders’ Meeting of May 11, 2017, at a price representing a discount of 9.94% compared to the volume-weighted average of the last twenty trading days preceding the decision of the Chief Executive Officer (€ 5.35) and 4.53% compared to the closing price of June 16, 2017 (€ 5.08).

The capital increase is carried out through the issuance of ordinary shares without preferential subscription rights in favor of a category of beneficiaries. The settlement of the new shares issued in connection with the capital increase and their admission to the Euronext Growth Paris exchange with Euronext Paris is scheduled for June 22, 2017. The new shares will bear current rights and will be admitted to trading on the Euronext Growth Paris exchange under ISIN code FR0004178572 – ALMED. The share capital of Medicrea will comprise 12,713,480 shares at the end of the settlement period. Thus, after the capital increase, the Company’s share capital has significantly changed. Post transaction, the holding of Orchard International and its executives is 19.17% of the total capital and the free float is 80.83%.

Midcap Partners acts as Lead Partner & Bookrunner of the Action.

EuroLand Corporate acted as a consultant to the Company.

In accordance with the provisions of Article 211-3 of the General Regulation of the AMF (Autorité des Marchés Financiers), the offer of the Company’s shares in connection with this capital increase for the benefit of a specific category of beneficiaries did not give rise to a submitted prospectus for the approval of the AMF. Detailed information about the Company, including its business activities, results and related risk profile, can be found in the Annual Financial Report for the year ended December 31, 2016, which is available for consultation, as well as other regulated information including press releases, on the Company’s website (www.medicrea.com).

Next financial publication: Sales for the 1st half of 2017: July 11, 2017, after market.

About Medicrea (www.Medicrea.com)

Through the lens of predictive medicine, Medicrea leads the design, integrated manufacture, and distribution of 30+ FDA approved implant technologies, utilized in over 100k spinal surgeries to date. Operating in a $10 billion marketplace, Medicrea is an SME with 175 employees worldwide, which includes 55 at its USA Corp. subsidiary in NYC. The Company has an ultra-modern manufacturing facility in Lyon, France housing the development and production of 3D-printed titanium patient-specific implants.

By leveraging its proprietary software analysis tools with big data and machine learning technologies supported by an expansive collection of clinical and scientific data, Medicrea is well-placed to streamline the efficiency of spinal care, reducing procedural complications and limiting time spent in the O.R.

For further information, please visit: www.medicrea.com.

Connect with Medicrea:
FACEBOOK | INSTAGRAM | TWITTER | WEBSITE | YOUTUBE

Medicrea is listed on
EURONEXT Growth Paris
ISIN: FR 0004178572
Ticker: ALMED

Caution

This press release is for informational purposes only. This press release does not constitute and cannot be regarded as an offer for public subscription or a solicitation of an interest in the public offering of financial securities. Dissemination of this press release in certain countries may constitute a violation of the legal provisions in force. The information contained in this press release does not constitute an offer of securities in France, the United States, Canada, Australia, Japan or any other country.

Contacts

The Medicrea Group
Denys Sournac
Founder, Chairman and CEO
dsournac@medicrea.com
or
Fabrice Kilfiger
Chief Financial Officer
fkilfiger@medicrea.com
Tel. : +33 (0)4 72 01 87 87