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., Promisemed Hangzhou Meditech Co., Ltd. and Owen Mumford, Ltd..

110
Total
110
Cleared
90d
Avg days
1981
Since
110 devices
49–72 of 110
Cleared May 19, 2022
Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)
K220370
Tianjin Huahong Technology Co., Ltd.
General & Plastic Surgery · 99d
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 Nov 06, 2017
gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler
K172712
Gri Medical & Electronic Technology Co., Ltd.
General & Plastic Surgery · 59d
Cleared May 12, 2016
Genteel Lancing Device
K153670
Genteel, LLC
General & Plastic Surgery · 143d
Cleared Feb 11, 2013
BABYLANCE HEEL INCISION DEVICE
K130132
Medipurpose Pte. , Ltd.
General & Plastic Surgery · 24d
Cleared Jul 13, 2012
PLANCET
K113513
Micropoint Technologies Pte, Ltd.
General & Plastic Surgery · 228d
Cleared Apr 18, 2012
ON CALL CHOSEN LANCING DEVICE
K113332
ACON Laboratories, Inc.
General & Plastic Surgery · 156d
Cleared Oct 21, 2010
SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250
K101145
Medipurpose Pte. , Ltd.
General & Plastic Surgery · 181d
Cleared Oct 19, 2010
BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200
K101417
Medipurpose Pte. , Ltd.
General & Plastic Surgery · 152d
Cleared Jul 23, 2004
L1-PRO SYSTEM
K041665
Pelikan Technologies, Inc.
General & Plastic Surgery · 35d
Cleared Apr 14, 2003
L1 SYSTEM
K024170
Pelikan Technologies, Inc.
General & Plastic Surgery · 117d
Cleared Aug 09, 2000
GOLDFINGER DEVICE
K001162
Mali-Tech , Ltd.
General & Plastic Surgery · 121d
Cleared Nov 17, 1994
FREE-LANCE
K944948
F.F.F. Enterprises, Inc.
General & Plastic Surgery · 41d
Cleared Nov 03, 1994
JENNINGS JAVELIN
K942548
Jfi Endineering, Inc.
General & Plastic Surgery · 156d
Cleared Jun 22, 1994
FEATHER-TOUCH SINGLE-STICK DEVICE
K942620
Ulster Scientific, Inc.
General & Plastic Surgery · 20d
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 Oct 15, 1993
CARELET SAFETY LANCET
K931828
Gainor Medical Europe, Ltd.
General & Plastic Surgery · 190d