Ingeneron, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ingeneron, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ingeneron, Inc. has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ingeneron, Inc. Filter by specialty or product code using the sidebar.
Ingeneron, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Oct 28, 2014
SMARTGRAFT 200 SYSTEM
General & Plastic Surgery
125d
Cleared
Sep 24, 2014
SMARTGRAFT 30 SYSTEM
General & Plastic Surgery
103d