Bego Bremer Goldschl?gerei Wilh. Herbst GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Bego Bremer Goldschl?gerei Wilh. Herbst GmbH & Co. KG - FDA 510(k) Cl...
Recent clearances: VarseoSmile TriniQ, VarseoSmile Crown plus
2
Total
2
Cleared
0
Denied
Bego Bremer Goldschl?gerei Wilh. Herbst GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Bremen, DE.
Last cleared in 2023. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bego Bremer Goldschl?gerei Wilh. Herbst GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bego Bremer Goldschl?gerei Wilh. Herbst GmbH & Co. KG
2 devices