Spinevision S.A.
Country not established
- Devices
- 5
What Spinevision S.A. makes
Spinevision S.A. manufactures spinal fixation systems, including the Lumis cannulated polyaxial pedicle screw fixation system and the U.L.I.S. polyaxial pedicle screw fixation system. The company also produces interbody fusion devices, specifically the SpaceVision PLIF, OLIF, and TLIF systems.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spinevision S.A. have in the registry?
The registry currently lists 5 devices for Spinevision S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spinevision S.A.'s devices?
Among its 5 most recently registered devices, Spinevision S.A. has devices listed in FDA 510(k) (5 devices).
What risk classes do Spinevision S.A.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Spinevision S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spinevision S.A. in the registry?
The most recently registered devices listed for Spinevision S.A. include SPINEVISION LUMIS(TM) CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S.(TM) POLYAXIAL PEDICLE ..., SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF, SPINEVISION LUMIS CANNULATED POLYAXIAL PEDICLE SCREW FIXATION SYSTEM, SPINEVISION U.L.I.S. POLYAXIAL PEDICLE SCREW FIXAT and LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System.