FDA applicant
Daum Corp.
FDA records 10 decisions for Daum Corp. (Crofton, MD) from 1997 to 2001: 10 510(k) clearances. Most are in product codes KNW (Instrument, Biopsy) and LNH (System, Nuclear Magnetic Resonance Imaging). No recall is linked to its devices.
FDA’s records also spell it “Daum GmbH”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Daum Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Daum Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Daum Corp.’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