# Inbella Medical, Inc.

- Location (FDA's records): Richmond Hill, CA
- FDA decisions: 5 (2025–2026): 5 510(k) clearances
- Names in FDA's records: Inbella Medical, Inc. (4); Inbella Medical , Ltd. (1)
- Product codes: GEI (5)
- 510(k) review time since 2016: median 30 days, against 113 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 7 (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
- InMode, Ltd.: 6 (https://510kreport.com/company/inmode)
- Inmode MD, Ltd.: 1 (https://510kreport.com/company/inmode-md)

## Recent decisions
- K251435: InbellaIgnite RF System (Jan 27, 2026)
- K252367: InbellaMulti System (Oct 15, 2025)
- K252215: InbellaMAX System (Jul 25, 2025)
- K250200: InbellaBody System (Feb 11, 2025)
- K243737: Inbella RF System (Jan 3, 2025)

Source page: https://510kreport.com/company/inbella-medical