Sie Ag,Surgical Instument Engineering is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sie Ag,Surgical Instument Engineering - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sie Ag,Surgical Instument Engineering has 1 FDA 510(k) cleared medical devices. Based in Greenwood Village, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Sie Ag,Surgical Instument Engineering Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sie Ag,Surgical Instument Engineering
1 devices