Remicalm, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Remicalm, LLC makes
Remicalm, LLC manufactures the TRIMIRA OCS 3000 and the TRIMIRA IDENTAFI 3000 medical devices.
Both devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Trimira Ocs 3000 Ref K082603
Regimes: 510(k) Registry: 510(k)Trimira Identafi 3000 Ref K090135
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Remicalm, LLC have in the registry?
The registry currently lists 2 devices for Remicalm, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remicalm, LLC's devices?
Among its 2 most recently registered devices, Remicalm, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Remicalm, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Remicalm, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Remicalm, LLC in the registry?
The most recently registered devices listed for Remicalm, LLC include TRIMIRA OCS 3000 and TRIMIRA IDENTAFI 3000.