Tyrx, Inc. is one of 4896 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyrx, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Tyrx, Inc. has 5 FDA 510(k) cleared medical devices. Based in Monmouth Junction, US.
Historical record: 5 cleared submissions from 2010 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tyrx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tyrx, Inc.
5 devices
Cleared
Nov 17, 2015
TYRX Neuro Antibacterial Envelope
General & Plastic Surgery
60d
Cleared
Nov 26, 2013
AIGIS RX N (MEDIUM), AIGIS RX N (LARGE)
General & Plastic Surgery
89d
Cleared
Jul 10, 2013
AIGIS RX N MEDIUM
General & Plastic Surgery
90d
Cleared
May 20, 2013
AIGIS RX R PM/ AIGIS RX R ICD
General & Plastic Surgery
46d
Cleared
Mar 26, 2010
PIVIT A/B ST AND PIVIT A/B ST-R
General & Plastic Surgery
130d