K251100
- 510(k) number
- K251100
- Device name
- IPGTFL-02
- Applicant
- Ipg Medical Corporation MA · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-09-19
- Date received
- 2025-04-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K251100.pdf
Official FDA record: K251100
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.