Inbella Medical, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Inbella Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InbellaIgnite RF System, InbellaMulti System, InbellaBody System
4
Total
4
Cleared
0
Denied
Inbella Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Richmond Hill, CA.
Latest FDA clearance: Jan 2026. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Inbella Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Inbella Medical, Inc.
4 devices