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KetoBM KBM-L1

by Ketobm LLC

KetoBM KBM-L1 is a Class II device made by Ketobm LLC, listed in FDA GUDID since 21 Nov 2022 (UDI-DI 00860001641738), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860001641738 UDI-DI Date21 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
KetoBM
Generic name
Blood lancet, single-use
Model / reference
KBM-L1
Primary DI / UDI-DI
00860001641738
FDA product code
QRL, QRK
GMDN term
Blood lancet, single-use
Device class
Class II
Regulation number
878.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood lancet, single-use

Similar devices in this category

Other devices filed under Blood lancet, single-use.

Other devices from Ketobm LLC

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)