Identity
- Trade Name
- Key Surgical Mr. Clear Anti-Fog FDA UDI
- Generic Name
- Endoscope antifog solution FDA UDI
- Device Name
- Key Surgical Mr. Clear Anti-Fog is indicated for use during endoscopic, laparoscopic, gastroscopic, and arthroscopic procedures, as well as any other procedures which require the use of an endoscope device, to prevent fogging of the endoscope lens. FDA UDI
- Model / Reference
- AF-031 FDA UDI
- Description
- Key Surgical Mr. Clear Anti-Fog is indicated for use during endoscopic, laparoscopic, gastroscopic, and arthroscopic procedures, as well as any other procedures which require the use of an endoscope device, to prevent fogging of the endoscope lens. FDA UDI
Identifiers
- Catalog Number
- AF-031 FDA UDI
- Primary DI / UDI-DI
- 00849771037859 FDA UDI
- 510(k) Number
- K993604 FDA UDI
- FDA Product Code
- OCT FDA UDI
- GMDN Term
- Endoscope antifog solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 6 Milliliter FDA UDI
Category: Endoscope antifog solution
Key Surgical Mr. Clear Anti-Fog by Key Surgical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscope antifog solution.
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Flo-X — Minimally Invasive Devices, LLC · Class II
- ClearIt Anti-Fog Kit — PRESERVATION SOLUTIONS, INC. · Class II
- Devon — Cardinalhealth · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- ArcRoyal Anti-Fog, Regular Solution, Sterile — Aspen Surgical Products, Inc. · Class II
- Clearify — Covidien LP · Class II
- Anti-Fog w/ Pad — XODUS MEDICAL, 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
- Key Surgical, LLC
Sources (1)
- FDA UDI c3589d7b-2c0a-4e84-ae0d-4a46bc88b4e5 36 fields · synced May 30, 2026