Sie Ag,Surgical Instrument Engineering is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Sie Ag,Surgical Instrument Engineering - FDA 510(k) Cleared Devices
Recent clearances: FEMTO LDV Z8 Femtosecond Surgical Laser
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.
510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sie Ag,Surgical Instrument Engineering
2 devices