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Diode Laser Therapy Systems (WLA-02)
FDA 510(k)Class II (US FDA 510(k))
510(k) K252599
Identifiers
- 510(k) Number
- K252599 FDA 510(k)
- FDA Product Code
- GEX FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4810 FDA 510(k)
- Regulation Number
- 878.4810 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Diode Laser Therapy Systems (WLA-02) by Wingderm Electro-Optics Ltd. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K252599 | Class II | Active |
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Manufacturer
- Manufacturer
- Wingderm Electro-Optics Ltd.
- FDA Applicant
- Wingderm Electro-Optics , Ltd.
Sources (1)
- FDA 510(k) K252599 24 fields · synced Jun 18, 2026