Identity
- Trade Name
- renu fresh multi-purpose solution FDA UDI
- Generic Name
- Multi-purpose soft contact lens solution FDA UDI
- Device Name
- Soft Contact Lens Disinfecting Solution, 4 FL OZ FDA UDI
- Model / Reference
- FCP-4122 FDA UDI
- Description
- Soft Contact Lens Disinfecting Solution, 4 FL OZ FDA UDI
Identifiers
- Catalog Number
- 623118 FDA UDI
- Primary DI / UDI-DI
- 00310119031186 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Multi-purpose soft contact lens solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multi-purpose soft contact lens solution
renu fresh multi-purpose solution by Bausch & Lomb Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multi-purpose soft contact lens solution.
- PREMIER — PHARMACY VALUE ALLIANCE, LLC · Class II
- Equate — Walmart Stores · Class II
- PREMIER — PHARMACY VALUE ALLIANCE, LLC · Class II
- REVITALENS — Johnson & Johnson Surgical Vision, Inc. · Class II
- COMPLETE — Johnson & Johnson Surgical Vision, Inc. · Class II
- HydroPure — OTE' NORTH AMERICA LLC. · Class II
- ACUVUE REVITALENS MPDS — Johnson & Johnson Surgical Vision, Inc. · Class II
- Nexus Optical — NEXUS OPTICAL, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bausch & Lomb Incorporated
Sources (1)
- FDA UDI c2119ed5-947b-49a2-9a95-c5b60873a56f 34 fields · synced Jun 8, 2026