Medical Device Manufacturer · US , Alpharetta , GA

Visioneering Technologies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Visioneering Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Alpharetta, US.

Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Visioneering Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Visioneering Technologies, Inc.

2 devices

1-2 of 2