Genii, Inc. is one of 5171 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genii, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Genii, Inc. has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Genii, Inc. Filter by specialty or product code using the sidebar.
Genii, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Sep 26, 2013
GENII ARC SMART ARGON PROBE
General & Plastic Surgery
170d
Cleared
Mar 22, 2012
GENII GI 4000 ELECTROSUGICAL GENERATOR
General & Plastic Surgery
139d