Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti is one of 54 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti - FDA 510(k) Cleared...
Recent clearances: Nucleoss Tpure Implant System
1
Total
1
Cleared
0
Denied
Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti has 1 FDA 510(k) cleared medical devices. Based in Bolgesi Tekeli, TR.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Registrar Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti
1 devices