FMK · Class II · 21 CFR 878.4850

FDA Product Code FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Single-use lancets with integrated sharps protection represent a significant advance in patient and healthcare worker safety. FDA product code FMK covers disposable blood lancets with integral sharps protection for single use.

These devices have a retractable or permanently shielded blade that is exposed only during the lancing action, preventing needle-stick injuries after use. They are used for capillary blood sampling in glucose monitoring and other point-of-care tests.

FMK devices are Class II medical devices, regulated under 21 CFR 878.4850 and reviewed by the FDA General & Plastic Surgery panel.

Leading manufacturers include Tianjin Huahong Technology Co., Ltd., Owen Mumford, Ltd. and Promisemed Hangzhou Meditech Co., Ltd..

109
Total
109
Cleared
91d
Avg days
1981
Since
109 devices
49–72 of 109
Cleared May 19, 2022
Accu-Chek Safe-T-Pro Plus Lancing Device
K220849
Roche Diabetes Care, Inc.
General & Plastic Surgery · 57d
Cleared May 18, 2022
gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler
K220917
Gri-Alleset, Inc.
General & Plastic Surgery · 49d
Cleared May 17, 2022
Heel Stick Safety Lancet (HHZ-II, HHZ-III)
K220372
Tianjin Huahong Technology Co., Ltd.
General & Plastic Surgery · 97d
Cleared Apr 05, 2022
Accu-Chek Safe-T-Pro Uno Lancing Device
K220364
Roche Diabetes Care, Inc.
General & Plastic Surgery · 56d
Cleared Aug 26, 2021
Heel Incision Safety Lancet
K210745
SteriLance Medical (Suzhou), Inc.
General & Plastic Surgery · 167d
Cleared Dec 03, 2019
Promisemed Heel Blood Lancet
K193009
Promisemed Hangzhou Meditech Co., Ltd.
General & Plastic Surgery · 36d
Cleared Dec 02, 2019
Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet
K192666
Promisemed Hangzhou Meditech Co., Ltd.
General & Plastic Surgery · 68d
Cleared Apr 18, 2012
ON CALL CHOSEN LANCING DEVICE
K113332
ACON Laboratories, Inc.
General & Plastic Surgery · 156d
Cleared Feb 10, 1994
SOFTTOUCH II LANCET DEVICE
K931258
Boehringer Mannheim Corp.
General & Plastic Surgery · 335d
Cleared Oct 19, 1993
BABISTICK
K933365
Graphic Controls Corp.
General & Plastic Surgery · 102d
Cleared Sep 29, 1993
MONOJECT(R) MONOLETTOR SAFETY LANCET
K932785
Sherwood Medical Co.
General & Plastic Surgery · 112d
Cleared Jul 23, 1993
B-D ULTRA FINE(R) LANCET
K932725
Bd Becton Dickinson Vacutainer Systems Preanalytic
General & Plastic Surgery · 46d
Cleared Jan 22, 1993
TENDERLETT FINGER
K923302
International Technidyne Corp.
General & Plastic Surgery · 200d
Cleared Jul 17, 1991
TENDERFOOT(R), MODIFICATION
K911997
International Technidyne Corp.
Hematology · 86d
Cleared Aug 02, 1990
GLUCOLET 2 AUTOMATIC LANCING DEVICE FOR OB. BLOOD
K902430
Heraeus Kulzer, Inc.
General & Plastic Surgery · 63d
Cleared Dec 01, 1988
TENDERFOOT
K883968
International Technidyne Corp.
Hematology · 72d
Cleared Feb 11, 1986
GLUCOLET AUTOMATIC LANCING DEVICE FOR OBT. BLOOD
K855203
Miles Laboratories, Inc.
General & Plastic Surgery · 47d
Cleared Jan 03, 1986
CHURCHHILL LANCET
K854760
Churchill Corp.
General & Plastic Surgery · 37d
Cleared Jun 11, 1984
STERILE BLOOD LANCETS
K841677
Abco Dealers, Inc.
General & Plastic Surgery · 49d
Cleared Jan 14, 1983
PRICK-TEST NEEDLE
K823760
Cordis Corp.
General & Plastic Surgery · 31d
Cleared Aug 27, 1982
AUTOLANCET
K822209
Bd Becton Dickinson Vacutainer Systems Preanalytic
General & Plastic Surgery · 32d
Cleared Mar 10, 1982
MONOJECTOR MONOLET LANCER
K820333
Sherwood Medical Co.
General & Plastic Surgery · 30d