Medical Device Manufacturer · CH , Port

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

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
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.

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