Envision Surgical System, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Envision Surgical System, Inc. makes
Envision Surgical System, Inc. manufactures the Envision Arthroscopy System along with its associated components, including the Envision Arthroscope, cannula, trocar, obturator, and probe, as well as the Envision Arthroscopy Visualization System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Envision Arthroscopy System Ref K942081
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Envision Arthroscopy Visualization System Ref K943666
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Envision Surgical System, Inc. have in the registry?
The registry currently lists 3 devices for Envision Surgical System, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Envision Surgical System, Inc.'s devices?
Among its 3 most recently registered devices, Envision Surgical System, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Envision Surgical System, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Envision Surgical System, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Envision Surgical System, Inc. in the registry?
The most recently registered devices listed for Envision Surgical System, Inc. include ENVISION ARTHROSCOPY SYSTEM, ENVISION ARTHROSCOPE, CANNULA, TROCAR, OBTURATOR, AND PROBE and ENVISION ARTHROSCOPY VISUALIZATION SYSTEM.