Repex Intl., Inc.
New ZealandFDA applicant, unverified
- Devices
- 1
What Repex Intl., Inc. makes
Repex Intl., Inc. manufactures the Repex Repeated Endrange Passive Exercise Machine, a Class I device designed for passive range-of-motion therapy to maintain joint flexibility and mobility in patients.
This product is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Repex-Repeated Endrange Passive Exercise Machine Ref K925271
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Repex Intl., Inc. have in the registry?
The registry currently lists 1 device for Repex Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Repex Intl., Inc.'s devices?
Among its 1 most recently registered device, Repex Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Repex Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Repex Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Repex Intl., Inc. in the registry?
The most recently registered devices listed for Repex Intl., Inc. include REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE.