K241771
- 510(k) number
- K241771
- Device name
- Liftendo; Liftendo 2.0
- Applicant
- Medical San Indústria DE Equipamentos Médicos Ltda. BR
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-09-16
- Date received
- 2024-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K241771.pdf
Official FDA record: K241771
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.