Replam Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Replam Corp. makes
Replam Corp. manufactures hydroxyapatite-based medical devices, including products named Replam Hydroxyapatite and Replam Hydroxyapatatite.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Replam Hydroxyapatite Ref K830304
Regimes: 510(k) Registry: 510(k)Replam Hydroxyapatatite Ref K822420
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Replam Corp. have in the registry?
The registry currently lists 2 devices for Replam Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Replam Corp.'s devices?
Among its 2 most recently registered devices, Replam Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Replam Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Replam Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Replam Corp. in the registry?
The most recently registered devices listed for Replam Corp. include REPLAM HYDROXYAPATITE and REPLAM HYDROXYAPATATITE.