Apex Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apex Medical Technologies, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Apex Medical Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 8 cleared submissions from 1987 to 2012. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Apex Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apex Medical Technologies, Inc.
8 devices
Cleared
May 24, 2012
RHEA CUP
Obstetrics & Gynecology
301d
Cleared
May 09, 2006
SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM
General Hospital
34d
Cleared
Jan 05, 1996
SEMINAL FLUID COLLECTION KIT II
Obstetrics & Gynecology
79d
Cleared
May 04, 1995
EXTRA PROTECTION POLYURETHANE CONDOM
Obstetrics & Gynecology
1064d
Cleared
Mar 18, 1993
APEX SPECIMEN BAG
Microbiology
55d
Cleared
Mar 06, 1991
POLYURETHANE CONDOM
Obstetrics & Gynecology
246d
Cleared
Mar 01, 1989
SENSATIONS BRAND CONDOMS
Obstetrics & Gynecology
695d
Cleared
Dec 14, 1987
HI-TOUCH (TM) BRAND SURGICAL GLOVES
General Hospital
41d