FDA applicant
Dhd Medical Products Div. Diemolding Corp.
FDA records 43 decisions for Dhd Medical Products Div. Diemolding Corp. (Canastota, NY) from 1979 to 1988: 43 510(k) clearances. Most are in product codes BZA (Connector, Airway (Extension)) and BYH (Drain, Tee (Water Trap)). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Dhd Medical Products Div. Diemolding Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dhd Medical Products Div. Diemolding Corp. since 2007.
Recalls per year
1in 2021
Class I Class II/III not classified
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