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ClearCam Kelling 1

by Clearcam, LLC 7 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB88303000002 UDI-DI Date21 May 2026ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ClearCam Kelling
Generic Name
Surgical instrument/endoscope cleaning utensil, single-use
Model / Reference
1
Primary DI / UDI-DI
B88303000002
510(k) Number
FDA Product Code
GCJ
GMDN Term
Surgical instrument/endoscope cleaning utensil, single-use
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K200228)

Other devices from Clearcam, LLC

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No