Medical Device Manufacturer · CH , Port

Sie Ag,Surgical Instrument Engineering - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Sie Ag,Surgical Instrument Engineering has 2 FDA 510(k) cleared medical devices. Based in Port, CH.

Last cleared in 2022. Active since 2015. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Sie Ag,Surgical Instrument Engineering Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Sie Ag,Surgical Instrument Engineering

2 devices

1-2 of 2