Ultracell Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ultracell Medical Technologies, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Ultracell Medical Technologies, Inc. has 24 FDA 510(k) cleared medical devices. Based in North Stonington, US.
Historical record: 24 cleared submissions from 1992 to 2001.
Browse the FDA 510(k) cleared devices submitted by Ultracell Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ultracell Medical Technologies, Inc.
24 devices
Cleared
Aug 24, 2001
ULTRACELL ABSORBENT STICK
Ophthalmic
42d
Cleared
Dec 17, 1997
ULTRACELL SUCTION SPONGE
Ophthalmic
156d
Cleared
Dec 17, 1997
ULTRACELL SUCTION SPONGE
General & Plastic Surgery
156d
Cleared
Dec 09, 1997
ULTRACELL NEURO SPONGES
Neurology
113d
Cleared
Nov 24, 1997
VISUAL ENDOSCOPIC NON-ALCOHOL ULTRACELL SPONGE (VENUS)
General Hospital
66d
Cleared
Nov 18, 1997
ULTRACELL PACKING WITH SLEEVE
Ear, Nose, Throat
92d
Cleared
Oct 01, 1997
ULTRACELL SUCTION SPONGE
General & Plastic Surgery
79d
Cleared
Apr 21, 1997
ULTRACELL NEURO SPONGES
Neurology
84d
Cleared
Aug 15, 1995
ULTRACELL NEURO SPONGES
Neurology
183d
Cleared
Apr 17, 1995
ULTRACELL ORTHOPEDIC SPONGES
General & Plastic Surgery
76d
Cleared
Apr 17, 1995
ULTRACELL ORTHOPEDIC SPONGES
General & Plastic Surgery
76d
Cleared
Apr 17, 1995
ULTRACELL ORTHOPEDIC SPONGES
General & Plastic Surgery
76d