FDA applicant
Resorba Medical GmbH
FDA records 4 decisions for Resorba Medical GmbH (Nuremberg, DE) from 2014 to 2018: 4 510(k) clearances. Most are in product codes GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid) and GAT (Suture, Nonabsorbable, Synthetic, Polyethylene). Its devices cite 17 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Resorba Medical GmbH’s devices, and how often a recall has named them.
FDA decisions per year
1in 2018
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2014.
Planning a device like Resorba Medical GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report