Owen Mumford, Ltd.

13 FDA 510(k) medical device clearances.

Top product codes for Owen Mumford, Ltd.

FMK — General, Plastic Surgery 5 devices
FMI — General Hospital 3 devices
KZH — General Hospital 2 devices
FMF — General Hospital 1 device
JKA — Clinical Chemistry 1 device
QRL — General, Plastic Surgery 1 device

Recent clearances by Owen Mumford, Ltd.

K223854 — Unistik® ShieldLock, Unistik VacuFlip JKA · 2023-06-30
K231124 — Unistik® 3 Single-Use Safety Lancets:- Extra (21G), Normal (23G), Comfort (28G), Gentle (30G) FMK · 2023-06-27
K222168 — Unistik TinyTouch Sterile Single-Use Heel Incision Safety Lancets - Preemie and Full-Term, Unistik Heelstik Sterile Single-Use Heel Incision Safety Lancets - MicroPreemie, Preemie, Full-Term and Toddler FMK · 2022-11-03
K222303 — Unistik® Pro FMK · 2022-10-25
K221613 — Freestyle Lancing Device II, Autolet, Autolet Lite, Unilet Lancets QRL · 2022-10-03
K222111 — Unistik Touch Single-Use Safety Lancets - 16G, 21G, 23G, 28G and 30G FMK · 2022-09-07
K221126 — Unistik® 3, sterile single-use safety lancets; Unistik® 3 Value, sterile single-use safety lancets; Abbott SF sterile single-use safety lancets FMK · 2022-08-12
K210399 — Unifine SafeControl FMI · 2021-09-17
K173881 — Unifine SafeControl 5mm x 30G, Unifine SafeControl 8mm x 30G FMI · 2018-07-11
K152339 — Unifine Pentips/ Unifine Pentips Plus FMI · 2016-06-24
K122837 — AUTOJECT 2 FOR GLASSY SYRINGE KZH · 2012-10-15
K011951 — EZ SYRINGE FMF · 2001-08-02
K000482 — MODIFICATION TO AUTOJECT MINI KZH · 2000-03-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.