Taut, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Taut, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Taut, Inc. has 16 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 16 cleared submissions from 1983 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Taut, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Taut, Inc.
16 devices
Cleared
Dec 13, 2002
ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244
General & Plastic Surgery
74d
Cleared
Aug 08, 2002
ADAPT OPEN ACCESS PORT, MODEL 41233
General & Plastic Surgery
76d
Cleared
Jun 22, 2001
TAUT BALLOON CATHETER, MODEL 50640
Gastroenterology & Urology
79d
Cleared
Feb 22, 2001
TAUT-INSUFFLATION NEEDLE
Obstetrics & Gynecology
83d
Cleared
Feb 22, 2001
ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP
General & Plastic Surgery
51d
Cleared
Oct 05, 1999
MINI-PORT
General & Plastic Surgery
36d
Cleared
Oct 05, 1999
INTRADUCER
General & Plastic Surgery
36d
Cleared
Dec 01, 1997
INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450
General & Plastic Surgery
179d
Cleared
Jul 18, 1996
TUAT SPLATTER CONTROL SHIELD SCS-300
General Hospital
57d
Cleared
Mar 20, 1996
INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8
General & Plastic Surgery
15d
Cleared
Feb 28, 1995
SPLATTER CONTROL SHIELD
General Hospital
112d
Cleared
Apr 06, 1993
OPERATIVE CHOLANGIOGRAM CATHETER
General & Plastic Surgery
187d
Cleared
Jul 15, 1992
INTRADUCER
General & Plastic Surgery
82d
Cleared
Feb 28, 1992
INTRADUCER
General & Plastic Surgery
53d
Cleared
Mar 08, 1988
O.P.C. INTRAVASCULAR CATHETER
General Hospital
90d
Cleared
Mar 29, 1983
PRE VUE
General Hospital
34d