Kensington Medical Holdings, LLC FG14-S

by Kensington Medical Holdings LLC

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860000950046 UDI-DI	Date13 Feb 2019Listed	StatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Kensington Medical Holdings, LLC
Generic Name: Device sterilization/disinfection container, reusable
Model / Reference: FG14-S

Primary DI / UDI-DI: 00860000950046
FDA Product Code: KCT
GMDN Term: Device sterilization/disinfection container, reusable

Device Class: Class II
Regulation Number: 880.6850
GUDID distribution status: Not in Commercial Distribution

Size: Length — 14 Inch

Properties

Lot / Batch Number

Other properties (13)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: 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