Ariste Medical’s hernia mesh combines synthetic material and proven antibiotics to address unmet need for one of America’s most common surgeries.
Ariste Medical, a pre-commercial drug+device company, has received 510(k) clearance (#K211132) from the U.S. Food and Drug Administration
PRIA Healthcare has partnered with Surgalign Holdings to expand access to Surgalign spine devices.
"We partnered with PRIA because of their extensive experience advocating for patients to receive favorable medical coverage," Terry Rich, Surgalign president and CEO said in a July 14 compa
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SAN CARLOS, Calif. , July 13, 2022 /PRNewswire/ -- Empirical Spine, Inc., a medical device company creating a new class of spinal implant that works in parallel with the natural structures of the spine to restore functionality and optimize qual
Six-month data for Nexxt Spine's Matrixx 3D-printed titanium interbody implant showed strong results compared to poly-ether-ether-ketone devices.
Six-month data showed a "significant increase" in fusion rates at one- and two-level cases compared to PEEK devices, according to a July 12 ne
Posted by admin on Jul 23rd, 2022
Stryker (NYSE:SYK – Get Rating) and G Medical Innovations (NASDAQ:GMVD – Get Rating) are both medical companies, but which is the better stock? We will contrast the two companies based on the strength of their risk, dividends, v
The implantable devices can be 3D printed for a customized fit, and contain sensors that track healing.
After spinal fusion surgery, patients typically receive spinal fusion cages to support the area during healing. However, these devices are one-size-fits-all solutions that don’t guar
Raymond Gardocki, MD, associate professor of Orthopaedic Surgery, played an instrumental role in developing and implanting the Flarehawk 9 — a first-of-its-kind interbody implant that can be placed endoscopically during spinal lumbar fusion surgery.
The patient Gardocki cared for had p
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VILLANOVA, Italy , July 13, 2022 /PRNewswire/ -- Limacorporate S.p.A., a global orthopedic company focused on digital innovation and patient-tailored hardware, and Orthofix Medical Inc, a global medical device company with a spine and orthoped
Spineart now has the green light from the FDA, with prized 510(k) clearances to market its new JULIET Ti lumbar interbody systems. As indicated in the July 18, 2016 news release, “The JULIET Ti PO, OL and TL interbody systems are the first range of titanium interbody implants benefiting from
Spineart is pleased to announce that it has received CE marking for its new JULIET®Ti lumbar interbody systems.
The JULIET®Ti PO, OL and TL interbody systems are the first range of Titanium interbody implants benefiting from our proprietary Ti-LIFETechnology1.
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