K260307
- 510(k) number
- K260307
- Device name
- Diode Laser Therapy Systems (V19)
- Applicant
- Weifang Mingliang Electronics Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2026-04-15
- Date received
- 2026-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K260307.pdf
Official FDA record: K260307
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.