Ultimed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ultimed, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Ultimed, Inc. has 8 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 8 cleared submissions from 2000 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ultimed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ultimed, Inc.
8 devices
Cleared
Jun 03, 2010
ULTICARE DISPOSABLE PEN NEEDLES
General Hospital
72d
Cleared
Jun 25, 2008
ULTIMED ULTICARE SAFETY SYRINGE
General Hospital
114d
Cleared
Jun 03, 2008
ULTIGUARD HOME INSULIN PEN NEEDLE DISPENSER AND SHARPS CONTAINER
General Hospital
11d
Cleared
Nov 29, 2006
ULTICARE DISPOSABLE SYRINGES AND NEEDLES
General Hospital
79d
Cleared
May 11, 2005
ULTRACARE DISPOSABLE PEN NEEDLES, MODELS 31 GAUGE X3/16, 29 GAUGE X 1/2
General Hospital
77d
Cleared
Dec 30, 2003
ULTICARE DISPOSABLE SYRINGE 3 ML/CC
General Hospital
25d
Cleared
Sep 16, 2002
ULTI GUARD HOME INSULIN SYRINGE CONTAINER
General Hospital
90d
Cleared
Mar 24, 2000
ULTICARE DISPOSABLE SYRINGE
General Hospital
99d