MedPlast Announces Agreement To Acquire Vention Medical Device Manufacturing Business

TEMPE, Ariz., Feb. 20, 2017 /PRNewswire/ — MedPlast, Inc., a global services provider to the medical device industry, announced today that it has signed a definitive agreement to acquire Vention Medical’s Device Manufacturing Services business.   The acquisition broadens MedPlast’s portfolio of capabilities and bolsters its position as a leading services provider to the world’s largest original equipment manufacturers.

MedPlast’s acquisition will further expand the company’s capabilities in assembly and packaging, enabling it to offer customers a comprehensive suite of services producing a wide range of medical products.  It also will extend MedPlast’s global footprint to 22 manufacturing facilities located in key markets throughout North and Central America, Asia and Europe.  Once complete, the acquisition will more than double MedPlast’s size.  The company will employ more than 3,500 engineers, technicians and assembly workers specializing in producing surgical, orthopedic, diagnostic and other medical devices.

“This acquisition will significantly strengthen MedPlast’s leadership position in the medical device manufacturing industry,” said MedPlast Chief Executive Officer Harold Faig.  “We will provide our customers a broad spectrum of integrated manufacturing capabilities and services from strategic locations around the world.  This is something our customers have been asking for, and we are committed to continuing to expand our capabilities in areas that will bring value to our customers.”

Bill Flaherty, president of Vention Medical’s Device Manufacturing Services business, added, “We are excited to come together with MedPlast.  We serve many of the same customers who will benefit from our combined offering and shared commitment to providing the highest quality standards and facilities in the industry.”

MedPlast’s acquisition comes two months after the company partnered with two investment firms to expand its offering.  JLL Partners, a middle-market private equity firm, and Water Street Healthcare Partners, a strategic investor focused exclusively on the health care industry, invested in MedPlast in December 2016.

“This is the first of what we expect will be more strategic acquisitions to build MedPlast into a market leader. Water Street and JLL are working closely with management to identify and pursue opportunities that will achieve MedPlast’s goal of offering customers a comprehensive, integrated portfolio of end-to-end product solutions,” said Kevin Swan, partner, Water Street.

The transaction is expected to close in the second quarter of 2017.  Financial terms of the agreement are not being disclosed.

About MedPlast
MedPlast is a global services provider to the medical device industry.  The company offers a range of engineering and manufacturing capabilities that support the world’s leading original equipment manufacturers with producing diagnostic, orthopedic, surgical and other medical products.  Headquartered in Tempe, Ariz., the company operates 11 ISO-certified facilities around the world.  For more information about MedPlast, visit medplastgroup.com.

About Vention Medical
Vention Medical is a global integrated solutions provider with more than 30 years of experience in design, engineering and manufacturing of complex medical devices and components.  Vention Medical specializes in molded components, and finished device assembly and packaging for the interventional and minimally invasive surgical markets.
Visit Vention at ventionmedical.com.

 

SOURCE MedPlast, Inc.

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SANUWAVE Announces Hiring of Andre Mouton as VP of International Sales and Relations

SUWANEE, GA–(Marketwired – Feb 21, 2017) – SANUWAVE Health, Inc. ( OTCQB : SNWV ) is pleased to announce the hiring of André Mouton to head the Company’s international sales and relations. SANUWAVE began a process 18 months ago of re-igniting their international efforts. This meant re-designing distribution agreements, restructuring partner economics, letting go of certain distributors, and adding new partners. The Company has also installed applicator refurbishment centers closer to the regions where the device is being used and this has had a strong acceptance among SANUWAVE’s customers. As SANUWAVE grows and expands on a country by country basis, the Company has found three models which work well for us: Distribution, Joint Ventures, and Exclusive Rights Agreements. Since the Company’s refocus on international sales the number of countries actively served has grown from 3 to 10, the number of device placements has tripled, and sales have increased as well.

Currently, SANUWAVE anticipates adding an additional 5 to 8 countries/regions in 2017. To assist in accelerating international growth and centralize the managing of the existing base the Company decided to bring on a senior level executive to streamline that process. SANUWAVE is pleased to announce André Mouton as the new VP of International Sales and Relations. André brings a strong history of growth and success in the healthcare community and deep relations globally. Kevin Richardson, SANUWAVE’s Acting CEO, stated, “André will allow us to manage and handle the massive growth and demand for SANUWAVE’s product internationally. His experience fits with the culture of solving the patients’ problems using shock wave technology.” André will also assist in the varied clinical work taking place internationally, which will in turn support all regions of the globe.

André has a background in Microbiology and obtained his MBA while working for a multi-national pharmaceutical group focusing on strategic marketing. He has resided in South Africa, Indonesia and Singapore and focused on business development and taking new products and services into the South East Asia (SEA) markets as well as Africa. He has held numerous senior positions with P&L responsibility as well as line management experience of staff of over 100 employees. He has assisted in numerous products entering new markets and was key to the process of adapting and entry strategy fit for local conditions and cultural acceptance.

André Mouton stated, “SANUWAVE is in a unique position to make a large impact on the global health community. The innovative dermaPACE® product helps to solve a problem stemming from an unfortunate worldwide epidemic, diabetes. As I have traveled the globe, I have seen firsthand how diabetes is not just an American disease, and in fact, growth rates are even greater in developing countries. With the dermaPACE device SANUWAVE will help these patients live a happier healthier life.”

About SANUWAVE Health, Inc.
SANUWAVE Health, Inc. (www.sanuwave.com) is a shock wave technology company initially focused on the development and commercialization of patented noninvasive, biological response activating devices for the repair and regeneration of skin, musculoskeletal tissue and vascular structures. SANUWAVE’s portfolio of regenerative medicine products and product candidates activate biologic signaling and angiogenic responses, producing new vascularization and microcirculatory improvement, which helps restore the body’s normal healing processes and regeneration. SANUWAVE applies its patented PACE technology in wound healing, orthopedic/spine, plastic/cosmetic and cardiac conditions. Its lead product candidate for the global wound care market, dermaPACE®, is CE Marked throughout Europe and has device license approval for the treatment of the skin and subcutaneous soft tissue in Canada, Australia and New Zealand. In the U.S., dermaPACE is currently under the FDA’s Premarket Approval (PMA) review process for the treatment of diabetic foot ulcers. SANUWAVE researches, designs, manufactures, markets and services its products worldwide, and believes it has demonstrated that its technology is safe and effective in stimulating healing in chronic conditions of the foot (plantar fasciitis) and the elbow (lateral epicondylitis) through its U.S. Class III PMA approved OssaTron® device, as well as stimulating bone and chronic tendonitis regeneration in the musculoskeletal environment through the utilization of its OssaTron, Evotron® and orthoPACE® devices in Europe, Asia and Asia/Pacific. In addition, there are license/partnership opportunities for SANUWAVE’s shock wave technology for non-medical uses, including energy, water, food and industrial markets.

Wenzel Spine Announces Acquisition of Interspinous & Facet Fixation Product Platforms

February 22, 2017

AUSTIN, Texas–(BUSINESS WIRE)–

Wenzel Spine, Inc., a medical technology company focused on providing minimally invasive solutions for the treatment of spinal disorders, today announced that it has completed the acquisition of the PrimaLOK™ SP Interspinous Fusion System and PrimaLOK™ FF Facet Fixation System from OsteoMed, LLC.

The PrimaLOK SP & FF platforms include a polyaxial interspinous process device and percutaneous facet screw system designed for MIS applications in treatment of lumbar spinal disorders. These patented technologies are designed to provide surgeons an expanded MIS solution when used in conjunction with the stand-alone, expandable, VariLift-LX interbody fusion device.

“This acquisition provides our distributors and surgeons a powerful combination of MIS solutions. When paired with our VariLift-LX stand-alone, expandable, interbody technology, surgeons now have the ability to provide supplemental fixation, when needed, without having to revert to pedicle screw constructs,” said Chad Neely, President and Chief Executive Officer of Wenzel Spine. “In addition, this expands our current product portfolio while strengthening our development pipeline and demonstrating our commitment to the development of innovative MIS solutions to our distribution and surgeon partners.”

Dr. Charles Gordon, the inventor of the PrimaLOK SP System, and founder of the Texas Spine & Joint Hospital, commented, “I am pleased that Wenzel Spine has added the PrimaLOK Systems to their product portfolio. We are very happy to be partnered with a Spine focused company and believe Wenzel Spine is the ideal partner to bring the full potential of the PrimaLOK Systems to market.” Dr. Gordon further commented, “There are tremendous MIS innovation opportunities in combining the advantages of the PrimaLOK and VariLift-LX technologies.”

Wenzel Spine plans to integrate the PrimaLOK platforms into the pipeline of innovative MIS solutions currently being developed. The company has completed a limited US release of the PrimaLOK SP & FF Systems and expects to offer wide US release of the products in the second quarter of 2017.

About Wenzel Spine, Inc.

Wenzel Spine, Inc. is a medical technology company focused on providing minimally invasive solutions for the treatment of spinal disorders. Headquartered in Austin, TX, Wenzel Spine is focused on delivering surgical solutions that improve the overall quality of spine care by simplifying procedures and reducing recovery time. Wenzel Spine seeks to improve patient quality of life by designing and producing devices of the highest quality to support our surgeon clients in the care and treatment of their patients. For more information about the company and our products, visit www.wenzelspine.com

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View source version on businesswire.com: http://www.businesswire.com/news/home/20170222005421/en/

Stryker only needs state approval for Portage brownfield plan

By Malachi Barrett –  February 22, 2017

KALAMAZOO, MI — One final step remains to approve a brownfield plan for a $150 million Styker Instruments project in Portage.

The Kalamazoo County Board of Commissioners became the last local body to sign off on a County Brownfield Redevelopment Authority financing plan that allows Stryker to capture tax revenue to clean up and develop a 288-acre site. Commissioners voted unanimously to approve the plan during its Feb. 21 meeting, which now goes to the state, who has the final say.

Brent Lalomia, vice president of quality and facilities, told the authority Thursday that the proposal for Stryker’s medical instruments division involves 485,000 square feet of facilities that will include three-stories of office space for sales, marketing and support functions connected to a two-story research and development lab. An atrium in the middle will house a customer experience center and functioning showroom.

Lalomia thanked the county brownfield authority for making the process efficient and collaborative.

The development is projected to retain 966 jobs and create an additional 105, a component of the plan lauded by Portage City Manager Larry Shaffer.

 

READ THE REST HERE

 

 

Active Implants Appoints Ted Davis President and Chief Executive Officer

February 22, 2017

MEMPHIS, Tenn.–(BUSINESS WIRE)–Active Implants, a company that develops orthopedic implant solutions, today announced that Ted Davis has been appointed president and chief executive officer. Davis succeeds Henry Klyce, who will continue as chairman of the board.

A current member of the Active Implants board, Davis has 25 years of experience in the life sciences industry as an investor and senior executive, including chief executive officer of MicroPort Orthopedics and president of its predecessor Wright Medical Technology’s global OrthoRecon division from 2012 through 2015. Prior to leading the carve out and integration of the OrthoRecon platform, Davis led Wright’s business development, corporate development and research & development functions from 2006 to 2012, with increasing responsibility for the business development, government affairs, national accounts, reimbursement, medical education and global research & development teams. Davis oversaw the acquisition and integration of a series of extremities and biologics platforms during Wright’s transformation into the market leader in the extremities market segment. Prior to joining Wright in 2006, Davis spent 10 years in the life sciences venture capital field, serving on the boards of multiple biotechnology and medical device companies while at MB Venture Partners and Vector Fund Management. He holds an MBA from the J.L. Kellogg Graduate School of Management at Northwestern University and a bachelor’s degree in engineering from Vanderbilt University.

“Ted’s expert business vision, along with his extensive experience providing strategy and leadership at orthopedic companies, makes him an extraordinary fit for Active Implants,” Klyce said. “A proven leader with a track record of delivering results, Ted brings the experience necessary to guide us through our next stage of growth.”

“I am honored and excited to lead Active Implants as we prepare for the next phase of development for the NUsurface Meniscus Implant around the world,” Davis said. “We have an opportunity to fulfill a significant unmet need in the orthopedic market here in the U.S. and worldwide, helping the millions of patients with persistent knee pain following meniscectomy. I look forward to continuing to work with Henry, given his successful track record in the orthopedics and spine medical technology industry and the outstanding progress he has led in the clinical development programs for the NUsurface Meniscus Implant here at Active Implants.”

The NUsurface® Meniscus Implant is an investigational treatment for patients with persistent knee pain following medial meniscus surgery. It is made from medical grade plastic and, as a result of its unique materials, composite structure and design, does not require fixation to bone or soft tissues. The NUsurface Meniscus Implant mimics the function of the natural meniscus and redistributes loads transmitted across the knee joint. The NUsurface Meniscus Implant has been used in Europe under CE Mark since 2008 and in Israel since 2011. Clinical trials are underway in the U.S., Europe and Israel to verify the safety and effectiveness of the NUsurface Meniscus Implant.

About Active Implants LLC

Active Implants LLC develops orthopedic implant solutions that complement the natural biomechanics of the musculoskeletal system, allowing patients to maintain or return to an active lifestyle. Active Implants is privately held with headquarters in Memphis, Tennessee. European offices are in Driebergen, The Netherlands, with R&D facilities in Netanya, Israel. For more information, visit www.activeimplants.com.

CAUTION Investigational device. Limited by United States law to investigational use.

Contacts

Merryman Communications
Joni Ramirez, 323-532-0746
joni@merrymancommunications.com

Senators Look to Overhaul Medical Device Inspections

By Michael Mezher – 21 February 2017

Sens. Johnny Isakson (R-GA) and Michael Bennett (D-CO) have introduced a bill that looks to dramatically alter the US Food and Drug Administration’s (FDA) process for inspecting device manufacturers.

Specifically, the bill calls for FDA to implement a more consistent, risk-based inspection process, as well as to improve communications with device makers regarding inspections and findings.

“The current device facility inspection process lacks transparency, predictability and consistency between facilities,” Isakson said. “This bill is designed to improve communication and consistency in the device facility inspections process, which will allow both FDA and device manufacturers to make more efficient use of resources.”

According to the bill, inconsistencies in how inspections are conducted across FDA’s foreign and domestic offices create challenges for device makers.

“The frequency and nature of inspections of device establishments are not consistently risk-based and a comprehensive, transparent, risk-based approach to inspections would result in greater focus on more significant risks to public health while reducing the burdens on establishments with a strong track record of compliance,” the bill states.

 

READ THE REST HERE

Dallas’ ‘Dr. Death’ gets life in prison over botched surgery

FoxNews.com

A Dallas jury sentenced a neurosurgeon dubbed “Dr. Death” by local media to life in prison on Monday, over his role in a botched back surgery that left his elderly patient crippled and in constant pain. Christopher Duntsch, 46, was arrested in July 2015 on five aggravated-assault charges after four of his patients were left crippled and two others died between July 2012 and June 2013, Dallas News reported.  

His trial focused on only one charge of injury to an elderly individual, with victim Mary Efurd testifying that she had trusted Duntsch to perform the 2012 procedure. Efurd, who was then 74, lost a third of her blood and the full use of her legs, Dallas News reported.

“I trusted that he would do what was right,” Efurd said, according to the report.

The 13-day trial included testimony from a doctor who treated Efurd after Duntsch’s procedure and said he found implants placed on muscle instead of bone, and a screw drilled into her spinal cavity.

“It’s as egregious as you can imagine,” Dr. Robert Henderson said, according to Dallas News.  

Jurors heard from other patients, including one who woke from surgery paralyzed from the neck down, another who passes out from chronic pain and a third who talks in a permanent whisper after she was left with a puncture wound in her throat.

 

READ THE REST HERE

American Academy of Orthopaedic Surgeons names Thomas E. Arend, Jr. as new CEO

ROSEMONT, Ill., Feb. 21, 2017 /PRNewswire-USNewswire/ — The American Academy of Orthopaedic Surgeons (AAOS) announced the selection of Thomas E. Arend, Jr., CAE, to the position of Chief Executive Officer, effective April 1, 2017. As CEO, Arend will work directly with the AAOS Board of Directors and executive management team to oversee a staff of 250 and manage an annual budget of $60 million.

“The Academy is very pleased that Tom Arend, an experienced and proven health care leader, will serve as our next CEO,” said AAOS President Gerald R. Williams Jr., MD. “Tom is a strong strategic thinker and visionary leader who understands the complexities of the changing health care arena. He will serve our members and staff well.”

Arend currently serves as Executive Vice President, Chief Operating Officer and General Counsel at the American College of Cardiology (ACC), a 52,000-member organization in Washington, DC. In this role, he is responsible for ensuring the ACC’s overall financial health, operational effectiveness and strategic direction. In addition, he is responsible for all aspects of the College’s legal, risk management and compliance activities.

Since joining the ACC in 2004, Arend has led the College through two CEO transitions and played critical roles in the development of comprehensive relationship with industry standards and code of ethics, as well as the College’s  five-year strategic plan and more recent governance restructuring.  Arend has also spearheaded several successful collaborations with other medical societies and stakeholders that directly benefit the ACC’s mission to transform cardiovascular care and improve heart health. Most recently, he was responsible for the addition of hospital accreditation services to the ACC’s suite of hospital quality improvement offerings.

“I am excited to join the AAOS, and I am honored and humbled to be leading this strong and vibrant organization,” said Arend. “I look forward to advancing the mission of the Academy and working closely with the volunteer leaders, members and staff.”

Prior to joining ACC, Arend served as an attorney at Shaw Pittman, LLP and Jenner & Block. He received a Juris Doctor degree from the Washington College of Law at The American University, a Master of Arts in International Law and Diplomacy from The Fletcher School of Law and Diplomacy at Tufts University, and a Bachelor of Arts from Kenyon College. He is a member of the Maryland and District of Columbia Bar associations, the American Society of Association Executives and the American College of Healthcare Executives.

Arend is replacing AAOS CEO Karen L. Hackett, FACHE, CAE, who is retiring after 14 years at the organization’s helm. The AAOS Board of Directors retained executive search firm Korn Ferry to lead the search for a new CEO.

About the AAOS
With more than 39,000 members, the American Academy of Orthopaedic Surgeons is the world’s largest medical association of musculoskeletal specialists. The AAOS provides educational programs for orthopaedic surgeons and allied health professionals, champions and advances the highest quality musculoskeletal care for patients, and is the authoritative source of information on bone and joint conditions, treatments and related issues.

Visit AAOS at:
Newsroom.aaos.org for bone and joint health news, stats, facts, images and interview requests.
ANationinMotion.org for inspirational patient stories, and orthopaedic surgeon tips on maintaining bone and joint health, avoiding injuries, treating musculoskeletal conditions and navigating recovery.
Orthoinfo.org for patient information on hundreds of orthopaedic diseases and conditions.

SOURCE American Academy of Orthopaedic Surgeons

Stryker Presents First K9s For Warriors Donation At The Honda Classic

MAHWAH, N.J., Feb. 21, 2017 /PRNewswire/ — Stryker Orthopaedics is pleased to announce its second PGA TOUR stop of 2017 with a first-ever appearance at The Honda Classic in Palm Beach Gardens, FL. Throughout the tournament, Stryker will further its commitment to joint health and to the nation’s military through a series of engaging activities for fans and tournament goers. On Thursday, Stryker will host a special K9s For Warriors ceremony, presenting one military hero with a service dog – Stryker’s first official canine sponsorship donation of the year.

As an extension of a successful relationship that began last year, in 2017 Stryker will continue to give a new leash on life to military heroes by sponsoring service canines and empowering veterans to return to civilian life with dignity and independence. Tournament goers can also show their support to veterans by purchasing the same hat that PGA TOUR professionals and longtime brand ambassadors, Fred Funk and Hal Sutton wear on TOUR at the newly renovated Mobility Zone – Stryker’s premiere “joint health” destination. With each hat purchase, Stryker will make a donation to the K9s For Warriors organization.

“This donation is just one of many ways in which we are honored to show our appreciation towards our nation’s veterans,” said Bill Huffnagle, President, Stryker’s Joint Replacement Division. “Stryker is proud to support our military and continue our mission to educate people about joint health and mobility in local communities across the nation.”

In addition to offering hats for sale to benefit K9s For Warriors, fans visiting The Mobility Zone will be able to learn about hip and knee pain and treatment options, as well as participate in fun, health inspired activities. Inside The Mobility Zone, fans can participate in the 2017 Stryker Challenge – a hands-on experience featuring Art H. Ritis, a life-size model that aims to provide tournament goers a basic understanding of joint replacement surgery and Stryker’s products. In addition, fans who stop by The Mobility Zone will be able to enter for a chance to win a trip for two to Atlanta, GA for the TOUR Championship® and walk inside the ropes as an honorary observer – a true VIP experience.1,2

Finally, to further demonstrate its commitment to motivating fans to stay active, Stryker will host the Health Walk at The Honda Classic. The Health Walk highlights joint health facts and tips along the course to educate fans as they follow their favorite golfers.

For a full list of tournaments stops, additional information on the Stryker Challenge as well as K9s For Warriors involvement, please visit: www.StrykerChallenge.com.

  1. Healthcare Professionals (HCPs) are not eligible to enter the Stryker Challenge Sweepstakes or participate in the any of these promotions. HCPs are defined as those individuals or entities involved in the provision of health care services and/or items to patients, which purchase, lease, recommend, use, arrange for the purchase or lease of, or prescribe Stryker’s products.
  2. No purchase necessary to enter or win Sweepstakes.  Void where prohibited by law.  For official rules visit StrykerChallenge.com.  Open to legal residents of the US & US Territories, 21+ as of date of entry.  Sweepstakes begins at 12:01 am ET on 1/11/17 and ends at 11:59 pm ET on 8/27/17.  Sponsored by Stryker.

About Stryker
Stryker is one of the world’s leading medical technology companies and, together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. Stryker is active in over 100 countries around the world.

About PGA TOUR
The PGA TOUR is the world’s premier membership organization for touring professional golfers, co-sanctioning more than 130 tournaments on the PGA TOUR, PGA TOUR Champions, Web.com Tour, PGA TOUR Latinoamérica, Mackenzie Tour-PGA TOUR Canada and PGA TOUR China.

GS Medical USA Announces New Product Portfolio and Company Enhancements

IRVINE, Calif., Feb. 20, 2017 /PRNewswire/ — GS Solutions Inc., DBA GS Medical USA (GSM), a global manufacturer and supplier of spinal implants, instrumentation and developer of high-quality surgical solutions, today announced several influential advancements for the organization. Following a strong close to the 2016 fiscal year, GSM is poised and prepared for an impactful, growth-oriented year in 2017.

“2017 begins anew for GS Medical with the regeneration of our ‘Expanding New Horizons’ concept,” remarks James Shin, CEO. “Our leadership team has worked tirelessly to lay the foundation for a unique infrastructure system which will continue to cultivate and foster new and existing relationships among our distributor colleagues, surgeons, industry contacts, and hospital partners.” Shin further mentions that many customers already engaged with GSM are excited about the direction and progression of the company.

GSM is pleased to announce the confirmed and pending launch of several products to their existing FDA 510k approved product portfolio. GSM currently offers products under the GSS™ and AnyPlus® product lines, and soon plans to launch the AnyPlus® Anterior Cervical Interbody Fusion (ACIF) implant and the AnyPlus® Dual-Lead Pedicle Screw System in March of 2017. This is in addition to the AnyPlus® Direct Lateral Interbody Fusion (DLIF) implant, slated for a Q2 2017 launch. “The company’s research and development team continues to focus on the essential needs of surgeon partners and their patients, thus yielding fundamental product design and manufacturing that fits the bill on a multitude of levels,” explains Shin. “The introduction of our comprehensive interbody line into the marketplace provides surgeons the option to select the appropriate implant that corresponds with the clinical indications of each individual patient,” states Chris Estuesta, Operations Manager at GSM.

With increased demand for the GS products, the company is also actively seeking distributor partnership opportunities. “Our sales team and industry partners are the lifeline of our company,” explains Adam Lampart, Director of US Sales. “We are always looking for qualified partners who desire to work with a company that is end-user focused, and delivers solid products with timely customer service.” For more information about distributor partner opportunities, please contact sales@gsmedicalusa.com.

About GS Medical USA
GS Medical features many spinal products spanning lumbar, thoracic and cervical applications. GSM products have been used in thousands of spine surgeries throughout the USA, and hundreds of thousands globally. Staffed with a network of industry leaders, medical sales distributors, accomplished engineers, and collaborating physicians, GSM is at the forefront of high-quality, value-added medical technology with a number of innovative implant solutions in the commercialization pipeline. Corporate headquarters are in Irvine, California and with international offices located in Seoul, Korea.

Media Relations Contact:
Amanda Collins
146989@email4pr.com
Phone: 831.477.1307 x213
FAX: 866.600.9712
6 Wrigley
Irvine, CA 92618

www.gsmedicalusa.com

SOURCE GS Medical USA

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