Vita Zahnfabrik GmbH H Rauter & CO is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vita Zahnfabrik GmbH H Rauter & CO - FDA 510(k) Cleared Devices
Recent clearances: VITA Akzent LC, VITA LUMEX AC, VITA Ambria
3
Total
3
Cleared
0
Denied
Vita Zahnfabrik GmbH H Rauter & CO has 3 FDA 510(k) cleared medical devices. Based in Bad Sackingen, DE.
Last cleared in 2021. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Vita Zahnfabrik GmbH H Rauter & 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 Zahnfabrik GmbH H Rauter & CO
3 devices