Orthoascent LLC
Country not established FDA establishment FEI 3032542289
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
- GUDID
Company details
- FDA FEI number
- 3032542289
- Address
- 9035 Wadsworth Pkwy Ste 1000, Westminster, CO, 80021
Frequently asked questions
How many devices does ORTHOASCENT LLC have in the registry?
The registry currently lists 3 devices for ORTHOASCENT LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHOASCENT LLC's devices?
Among its 3 most recently registered devices, ORTHOASCENT LLC has devices listed in FDA GUDID (3 devices).
What risk classes do ORTHOASCENT LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for ORTHOASCENT LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHOASCENT LLC in the registry?
The most recently registered devices listed for ORTHOASCENT LLC include ASCENT FLEXXPRP FG-001 Platelet Rich Plasma (PRP), ASCENT FLEXXBMC FG-002 Bone Marrow Concentrate (BMC) and BMC Device Masterpack FG-016 BMC Device Masterpack.