Identity
- Trade Name
- Polylase FDA UDI
- Generic Name
- Dermatological solid-state laser system FDA UDI
- Device Name
- Pulsed Alexandrite Laser FDA UDI
- Model / Reference
- AL FDA UDI
- Description
- Pulsed Alexandrite Laser FDA UDI
Identifiers
- Catalog Number
- Polylase AL FDA UDI
- Primary DI / UDI-DI
- 90860002307018 FDA UDI
- 510(k) Number
- K010715 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Dermatological 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dermatological solid-state laser system
Polylase by Ddc Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dermatological solid-state laser system.
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- GentleMax Pro — Candela Corporation · Class II
- CLARITY II — Lutronic Corporation · Class II
- GentleYAG — Candela Corporation · Class II
- Splendor X — Bios, Inc. · Class II
- Canister HFC-134a /980g, ALUM, 15 pack — Candela Corporation · Class II
- GentleYAG — Candela Corporation · Class II
Cleared under the same submission
K010715 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
- Ddc Technologies, Inc.
Sources (1)
- FDA UDI 03a07971-c2fa-47f5-8b4c-d9c34820ceb7 36 fields · synced Jun 1, 2026