Identity
- Trade Name
- Smooth Beauty Laser FDA UDI
- Generic Name
- Dermatological laser beam guiding handpiece FDA UDI
- Model / Reference
- SRL FDA UDI
Identifiers
- Catalog Number
- 3426 FDA UDI
- Primary DI / UDI-DI
- G7433426 FDA UDI
- 510(k) Number
- K130459 FDA UDI
- FDA Product Code
- ONG FDA UDI
- GMDN Term
- Dermatological laser beam guiding handpiece FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dermatological laser beam guiding handpiece
Smooth Beauty Laser by Tria Laser Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dermatological laser beam guiding handpiece.
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Cleared under the same submission
K130459 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Tria Laser Inc
Sources (1)
- FDA UDI 9f6b92bd-e27e-475f-87ce-53d951143b5b 35 fields · synced May 31, 2026