Medical Device Manufacturer · US , Elk Grove Village , IL

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

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Surgimatix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.

Last cleared in 2021. Active since 2014. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Surgimatix, Inc.

2 devices

1-2 of 2