Detax GmbH & Co. KG is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Detax GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Freeprint denture, FREEPRINT temp
5
Total
5
Cleared
0
Denied
Detax GmbH & Co. KG has 5 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.
Historical record: 5 cleared submissions from 2000 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Detax GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Consultancy B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Detax GmbH & Co. KG
5 devices