K252367
- 510(k) number
- K252367
- Device name
- InbellaMulti System
- Applicant
- Inbella Medical, Inc. CA
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-15
- Date received
- 2025-07-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K252367.pdf
Official FDA record: K252367
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.