K261602
- 510(k) number
- K261602
- Device name
- Eye Recovery Pro (PH-e03)
- Applicant
- Shenzhen Goodwind Technology Development Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2026-08-10
- Date received
- 2026-05-14
- 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: K261602.pdf
Official FDA record: K261602
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.