Vita Zanhnfabrik H. Rauter GmbH Co. is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vita Zanhnfabrik H. Rauter GmbH Co. - FDA 510(k) Cleared Devices
Recent clearances: VITA VIONIC Bond
1
Total
1
Cleared
0
Denied
Vita Zanhnfabrik H. Rauter GmbH Co. has 1 FDA 510(k) cleared medical devices. Based in Bad Sackingen, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Vita Zanhnfabrik H. Rauter GmbH Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vita North America as regulatory consultant.
FDA 510(k) Regulatory Record - Vita Zanhnfabrik H. Rauter GmbH Co.
1 devices