Medical Device Manufacturer · US , Austin , TX

Genii, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012

Total

Cleared

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. is one of 5656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Genii, Inc.

2 devices

1-2 of 2