K253134
- 510(k) number
- K253134
- Device name
- LAGIS Endoscopic Instruments- Scissors (EI-330S EI-330S-T EI-330MS EI-330MS-T)
- Applicant
- Lagis Enterprise Co., Ltd. TW
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-05-20
- Date received
- 2025-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253134.pdf
Official FDA record: K253134
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.