FDA applicant
Dhd Diemolding Healthcare Div.
FDA records 11 decisions for Dhd Diemolding Healthcare Div. (Canastota, NY) from 1991 to 1998: 11 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BWF (Spirometer, Therapeutic (Incentive)). 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 Diemolding Healthcare Div.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dhd Diemolding Healthcare Div. since 2007.
Recalls per year
1in 2021
Class I Class II/III not classified
Planning a device like Dhd Diemolding Healthcare Div.’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