Renovis Surgical Technologies
Country not established
- Devices
- 23
What Renovis Surgical Technologies makes
Renovis Surgical Technologies manufactures orthopedic implants for spinal and joint reconstruction, including hip replacement systems, lateral lumbar interbody fusion devices, knee arthroplasty components, and anterior cervical fusion systems. Their portfolio includes modular fusion cages, stand-alone fusion implants, and specialized spinal instrumentation designed for specific surgical approaches.
The company’s devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 23 devicesFrequently asked questions
How many devices does Renovis Surgical Technologies have in the registry?
The registry currently lists 23 devices for Renovis Surgical Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renovis Surgical Technologies's devices?
Among its 23 most recently registered devices, Renovis Surgical Technologies has devices listed in FDA 510(k) (23 devices).
What risk classes do Renovis Surgical Technologies's devices fall under?
Among its 23 most recently registered devices, the classes recorded for Renovis Surgical Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Renovis Surgical Technologies in the registry?
The most recently registered devices listed for Renovis Surgical Technologies include Renovis Surgical Hip Replacement System, RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM, Renovis S180 Lateral Lumbar Interbody Fusion System and S 100 PEDICLE SCREW SYSTEM.