Skip to content

ClearCam Kelling 1

by Clearcam, LLC 7 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 NumberB883SK300530113 UDI-DI Date5 May 2020ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 / Ref / Catalog
1, SK3005301
Primary DI / UDI-DI
B883SK300530113
FDA Product Code
GCJ
GMDN Term
Surgical instrument/endoscope cleaning utensil, single-use
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument/endoscope cleaning utensil, single-use

Other devices from Clearcam, LLC

Properties

  • Sterile
  • Single Use
  • Premarket Exempt

Other properties (11)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No