Sis Ag, Surgical Instrument Systems is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Sis Ag, Surgical Instrument Systems - FDA 510(k) Cleared Devices
Recent clearances: Galilei G6 Lens Professional
1
Total
1
Cleared
0
Denied
Sis Ag, Surgical Instrument Systems has 1 FDA 510(k) cleared medical devices. Based in Port, CH.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Sis Ag, Surgical Instrument Systems 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 - Sis Ag, Surgical Instrument Systems
1 devices