Inopro, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Inopro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IRRIGO Wound Wash Jet System
1
Total
1
Cleared
0
Denied
Inopro, Inc. has 1 FDA 510(k) cleared medical devices. Based in Cowansville, CA.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Inopro, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inopro, Inc.
1 devices