American Biomaterials Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Biomaterials Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
American Biomaterials Corp. has 6 FDA 510(k) cleared medical devices. Based in Princeton, US.
Historical record: 6 cleared submissions from 1985 to 1994.
Browse the FDA 510(k) cleared devices submitted by American Biomaterials Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Biomaterials Corp.
6 devices
Cleared
Jul 07, 1994
EVERT-O-CATH CATHETER
Cardiovascular
776d
Cleared
Feb 05, 1993
AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS
General & Plastic Surgery
137d
Cleared
Jan 29, 1993
HOLE PUNCH
General Hospital
396d
Cleared
Nov 18, 1988
BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINER
Dental
296d
Cleared
Nov 28, 1986
CREATIVE CARE SYSTEMS' IV START KIT
General & Plastic Surgery
60d
Cleared
Jan 09, 1985
BIOGLASS OSSICULAR RECONSTRUCTION PROSTH
Ear, Nose, Throat
126d