Applied Biomaterial Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Biomaterial Technologies - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Applied Biomaterial Technologies has 7 FDA 510(k) cleared medical devices. Based in Bremerton, US.
Historical record: 7 cleared submissions from 1990 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Applied Biomaterial Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Applied Biomaterial Technologies
7 devices
Cleared
Jan 31, 1995
DURALASTIC SHEETING
General & Plastic Surgery
439d
Cleared
Jan 31, 1995
DURALASTIC SHEETING
General & Plastic Surgery
82d
Cleared
Nov 17, 1994
THE PERMARIDGE MATRIX CHIN
General & Plastic Surgery
602d
Cleared
Feb 03, 1992
PEC IMPLANT
General & Plastic Surgery
165d
Cleared
Sep 12, 1990
ZYMALAR IMPLANT
General & Plastic Surgery
113d
Cleared
Sep 12, 1990
THE MAGNUM CHIN IMPLANT
General & Plastic Surgery
113d
Cleared
Aug 14, 1990
THE NAUTILUS NASAL IMPLANT
General & Plastic Surgery
84d