K262070
- 510(k) number
- K262070
- Device name
- Diode Laser Therapy Systems (DL612A)
- Applicant
- Hebei Zollvan Medical Technology Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2026-08-19
- Date received
- 2026-06-22
- 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: K262070.pdf
Official FDA record: K262070
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.