Osteomni Inc
United Statesfrom the FDA registration address FDA establishment FEI 3041915189
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Osteomni Inc makes
OSTEOMNI INC manufactures the OSTEOMNI SPINAL CAGES SYSTEM, which is a medical device used in spinal surgeries.
The OSTEOMNI SPINAL CAGES SYSTEM is classified as a Class II device and is listed in the FDA 510(k) registry. OSTEOMNI INC is based in the US.
Catalogue
Osteomni Spinal Cages System Ref K260850
Regimes: 510(k) Registry: 510(k)Osteomni Spinal Fixation System Ref K254247
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3041915189
- Address
- 3402 NW 73RD ST. STE# 3 MIAMI, FL 33147 US, Miami, FL, 33147
Frequently asked questions
How many devices does OSTEOMNI INC have in the registry?
The registry currently lists 2 devices for OSTEOMNI INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list OSTEOMNI INC's devices?
Among its 2 most recently registered devices, OSTEOMNI INC has devices listed in FDA 510(k) (2 devices).
What risk classes do OSTEOMNI INC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for OSTEOMNI INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from OSTEOMNI INC in the registry?
The most recently registered devices listed for OSTEOMNI INC include OSTEOMNI SPINAL CAGES SYSTEM and OSTEOMNI SPINAL FIXATION SYSTEM.