Identity
- Trade Name
- OptiLight™ Aesthetics FDA UDI
- Generic Name
- Intense pulsed light dry eye therapy unit FDA UDI
- Model / Reference
- OptiLight Aesthetics FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290117771006 FDA UDI
- FDA Product Code
- QIU FDA UDI
- GMDN Term
- Intense pulsed light dry eye therapy unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5201 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: Intense pulsed light dry eye therapy unit
OptiLight™ Aesthetics by Lumenis Be, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Intense pulsed light dry eye therapy unit.
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- Digital OptiLight Aesthetics — Lumenis Be, Inc. · Class II
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
- Lumenis Be, Inc.
Sources (1)
- FDA UDI efa597d5-6cda-49b1-894b-874b7fd84447 32 fields · synced Jun 1, 2026