Tactyl Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tactyl Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Tactyl Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Vista, US.
Historical record: 7 cleared submissions from 1990 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tactyl Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tactyl Technologies, Inc.
7 devices
Cleared
Apr 25, 1996
TACTYLON POWDER FREE EXAMINATION GLOVE
General Hospital
147d
Cleared
Apr 15, 1996
POWDER FREE TACTYLON SURGEONS GLOVE
General Hospital
140d
Cleared
Jan 26, 1996
LUBRICATED CONDOM
Obstetrics & Gynecology
178d
Cleared
Apr 13, 1995
TACTYLON(TM) POWDER FREE SURGEONS GLOVE
General Hospital
86d
Cleared
Dec 27, 1994
TACTYLON(TM) CONDOM
Obstetrics & Gynecology
1365d
Cleared
Nov 21, 1990
PATIENT EXAMINATION GLOVE/HYPOALLERGENIC
General Hospital
8d
Cleared
Jul 10, 1990
TACTYLON TM SURGICAL GLOVE
General Hospital
12d