Medical Device Manufacturer · US , Chesterfield , MO

Vortex Surgical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Vortex Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chesterfield, US.

Last cleared in 2022. Active since 2019. Primary specialty: Ophthalmic.

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

FDA 510(k) cleared devices by Vortex Surgical, Inc.

2 devices

1-2 of 2