Trinity Biotech, Plc is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trinity Biotech, Plc - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Trinity Biotech, Plc has 5 FDA 510(k) cleared medical devices. Based in Jamestown, US.
Historical record: 5 cleared submissions from 1999 to 2002. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Trinity Biotech, Plc Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trinity Biotech, Plc
5 devices
Cleared
Jan 24, 2002
CAPTIAM SYPHILIS-G ASSAY
Microbiology
29d
Cleared
Nov 08, 2001
UNI-GOLD STREP A TEST KIT
Microbiology
157d
Cleared
Nov 29, 2000
CAPTIA SYPHILIS-G ELISA TEST SYSTEM
Microbiology
197d
Cleared
Dec 21, 1999
UNI-GOLD H. PYLORI
Microbiology
217d
Cleared
Feb 11, 1999
UNI-GOLD STREP A TEST KIT
Microbiology
219d