# Armis Biopharma, Inc.

- Location (FDA's records): Fort Collins, CO
- FDA decisions: 2 (2020–2023): 2 510(k) clearances
- Product codes: HTY (1), FQH (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Extremity Medical, LLC: 1 (https://510kreport.com/company/extremity-medical)
- Paragon 28, Inc.: 1 (https://510kreport.com/company/paragon-28)
- Next Science, LLC: 1 (https://510kreport.com/company/next-science)

## Recent decisions
- K220759: Armis VeriCyn Wound Wash (May 25, 2023)
- K202777: VeriFixx™ Small Bone Implant (Nov 17, 2020)

Source page: https://510kreport.com/company/armis-biopharma
