Armis Biopharma, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Armis Biopharma, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Armis VeriCyn Wound Wash, VeriFixx™ Small Bone Implant
2
Total
2
Cleared
0
Denied
Armis Biopharma, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fort Collins, US.
Last cleared in 2023. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Armis Biopharma, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pharmatech Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Armis Biopharma, Inc.
2 devices