Armis Biopharma, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3020745223
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Armis VeriCyn Wound Wash Ref K220759
Regimes: 510(k) Registry: 510(k)VeriFixx™ Small Bone Implant Ref K202777
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020745223
- Address
- 2401 Research Blvd Ste 205, Fort Collins, CO, 80526
Frequently asked questions
How many devices does ARMIS BIOPHARMA, INC. have in the registry?
The registry currently lists 7 devices for ARMIS BIOPHARMA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ARMIS BIOPHARMA, INC.'s devices?
Among its 7 most recently registered devices, ARMIS BIOPHARMA, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ARMIS BIOPHARMA, INC.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for ARMIS BIOPHARMA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ARMIS BIOPHARMA, INC. in the registry?
The most recently registered devices listed for ARMIS BIOPHARMA, INC. include VeriCyn Wound Wash VWW-2001, VeriCyn Wound Wash VWW-2002, VeriCyn Wound Wash VWW-2003 and VeriCyn Wound Wash VWW-2005.