Ansell, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ansell, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Ansell, Inc. has 30 FDA 510(k) cleared medical devices. Based in Dothan, US.
Historical record: 30 cleared submissions from 1980 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ansell, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ansell, Inc.
30 devices
Cleared
Jul 21, 1999
ANSELL CONDOMS
Obstetrics & Gynecology
225d
Cleared
Jul 06, 1999
LIFESTYLES XTRA PLEASURE
Obstetrics & Gynecology
272d
Cleared
Dec 19, 1995
SPERMICIDALLY LUBRICATED CONDOM
Obstetrics & Gynecology
713d
Cleared
Sep 27, 1995
HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVE
General Hospital
70d
Cleared
Aug 07, 1995
HYPOALLERGENIC POWDERED AMBIDEXTROUS PATIENT EXAMINATION GLOVES
General Hospital
259d
Cleared
Mar 02, 1995
POWDER FREE, HYPOALLERGENIC AMBIDEXTROUS PATIENT EXAMINATION GLOVES
General Hospital
101d
Cleared
Jan 30, 1995
CONDOM
Obstetrics & Gynecology
390d
Cleared
Jan 30, 1995
NON-LUBRICATED CONDOM
Obstetrics & Gynecology
390d
Cleared
Mar 11, 1993
ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES
General Hospital
567d
Cleared
Jan 17, 1992
LATEX EXAMINATION GLOVES
General Hospital
87d
Cleared
Aug 29, 1990
PATIENT EXAM GLOVES (DUSTED W/USP STARCH POWDER)
General Hospital
51d
Cleared
Aug 29, 1990
PATIENT EXAM GLOVES (FINISH W/USP STARCH POWDER)
General Hospital
50d