Physio Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Physio Systems, Inc. makes
Physio Systems, Inc. manufactures rehabilitation and motion analysis devices, including the DISCIPLINE II RTD for real-time dynamic gait assessment, the DISCIPLINE I system for biomechanical analysis, and the VILLAN software for video-based gait and movement evaluation.
These products are regulated under FDA Class I and Class II classifications, with authorisation via the 510(k) pathway. The company’s devices are listed in the FDA’s 510(k) registry. Physio Systems, Inc. is based in the United States.
Catalogue
Discipline Ii Rtd Ref K871557
Regimes: 510(k) Registry: 510(k)Discipline I Ref K870872
Regimes: 510(k) Registry: 510(k)Villan (Video Lift Link Analysis) Ref K910712
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physio Systems, Inc. have in the registry?
The registry currently lists 3 devices for Physio Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physio Systems, Inc.'s devices?
Among its 3 most recently registered devices, Physio Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Physio Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Physio Systems, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physio Systems, Inc. in the registry?
The most recently registered devices listed for Physio Systems, Inc. include DISCIPLINE II RTD, DISCIPLINE I and VILLAN (VIDEO LIFT LINK ANALYSIS).