Apex Medical Technologies, Inc. is one of 22357 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
Recent clearances: RHEA CUP, SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM, SEMINAL FLUID COLLECTION KIT II
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.
510(k) submissions have been managed by Citech as regulatory consultant.
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