Freudenberg Technology Innovation SE & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Freudenberg Technology Innovation SE & Co. KG - FDA 510(k) Cleared De...
Recent clearances: scaffolene CL100 Bioresorbable Collagen Matrix
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Denied
Freudenberg Technology Innovation SE & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Weinheim, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Freudenberg Technology Innovation SE & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Parexel International as regulatory consultant.
FDA 510(k) Regulatory Record - Freudenberg Technology Innovation SE & Co. KG
1 devices