Identity
- Trade Name
- AlexLAZR FDA UDI
- Generic Name
- Dermatological frequency-doubled solid-state laser system FDA UDI
- Device Name
- Pulsed Laser FDA UDI
- Model / Reference
- 9914-00-2017 FDA UDI
- Description
- Pulsed Laser FDA UDI
Identifiers
- Catalog Number
- 9914-00-2017 FDA UDI
- Primary DI / UDI-DI
- 00817495022611 FDA UDI
- 510(k) Number
- K081324 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Dermatological frequency-doubled solid-state laser system 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
Yes
FDA UDI
Over-the-Counter
No
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
Yes
FDA UDI
Category: Dermatological frequency-doubled solid-state laser system
AlexLAZR by Candela Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K081324 also covers:
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- Alex TriVantage 1064 Handpiece Assembly — Candela Corporation
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- Alex TriVantage 532 Handpiece Assembly — Candela Corporation
- Alex TriVantage 532 PT Handpiece Assembly — Candela Corporation
- Alex TriVantage Delivery System — Candela Corporation
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Candela Corporation
Sources (1)
- FDA UDI 03469820-9407-40da-abec-d5e8b14855b2 36 fields · synced Jun 8, 2026