Plexus Intl., Inc.
Country not established
- Devices
- 1
What Plexus Intl., Inc. makes
Plexus Intl., Inc. manufactures the ORTHO-PLEX-REHABILITATION SYSTEM, a device designed for orthopedic rehabilitation purposes.
The company’s portfolio is regulated under Class I device classification in the U.S. and is listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Ortho-Plex-Rehabilitation System Ref K920686
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plexus Intl., Inc. have in the registry?
The registry currently lists 1 device for Plexus Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plexus Intl., Inc.'s devices?
Among its 1 most recently registered device, Plexus Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Plexus Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Plexus Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Plexus Intl., Inc. in the registry?
The most recently registered devices listed for Plexus Intl., Inc. include ORTHO-PLEX-REHABILITATION SYSTEM.