Ambulatory surgery centres (ASCs) are self-contained medical facilities that specialise in surgical, diagnostic, and preventive procedures that do not necessitate hospitalisation. The cost-effectiveness of ASCs saves governments, third-party payers, and...
Spinal Implants & Surgery Devices Market Research Report by Product Type (Cervical Fusion Devices, Non-Fusion Devices, and Spinal Decompression Devices), Type of Surgery, End User, Region (Americas, Asia-Pacific, and Europe,...
3D-Side Gains 510(k) for Ankle Arthroplasty Pre-Operative Planning After receiving a 510(k) clearance for its fully automated radiological image processing software, Customize, and its pre-operative planning for shoulder arthroplasty earlier this...
New expandable interbody enables up to a 34mm-wide footprint from a posterior approach with up to 2cm2 of bone graft contact area through the implant PALM BEACH GARDENS, Fla., Aug. 15, 2022...
On August 8, 2022, AxioMed LLC submitted to the FDA all the required documents for Module III. This is the final Module containing all the data tables comparing AxioMed to...
DEERFIELD, Ill., Aug. 09, 2022 (GLOBE NEWSWIRE) -- Surgalign Holdings, Inc., (NASDAQ: SRGA) a global medical technology company focused on elevating the standard of care by driving the evolution of...
NEW YORK, Aug. 10, 2022 /PRNewswire/ -- The "Ortho Pediatric Devices Market by Product and Geography - Forecast and Analysis 2022-2026" report by Technavio expects the market size to grow by USD 1.36...
U.S. clinical study will compare efficacy and safety of traditional mini-open carpal tunnel release and carpal tunnel release using UltraGuideCTR and real-time ultrasound guidance EAGAN, Minn., Aug. 9, 2022 /PRNewswire/ -- Sonex Health and The...
Lazurite’s ArthroFree™ System is the first wireless surgical camera system to receive FDA market clearance for arthroscopy and general endoscopy. (Photo: Business Wire)Lazurite™ Named One of the Top 100 Healthcare...
ARLINGTON, Tenn., Aug. 8, 2022 /PRNewswire/ -- MicroPort Navibot has received 510(K) clearance from the Food and Drug Administration (FDA) in the United States for the SkyWalker™ System, the company's first robot-assisted platform for...