Resilia, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Resilia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Uresta®
1
Total
1
Cleared
0
Denied
Resilia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Moncton, CA.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Resilia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QUARAS, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Resilia, Inc.
1 devices