# Dhd Diemolding Healthcare Div.

- Location (FDA's records): Canastota, NY
- FDA decisions: 11 (1991–1998): 11 510(k) clearances
- Product codes: CAF (5), BWF (3), BZA (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dhd Healthcare Corp.: 6 (https://510kreport.com/company/dhd-healthcare)
- Trudell Medical Int'L: 1 (https://510kreport.com/company/trudell-medical-int-l)
- Eumedics Medizintechnik Und Marketing GmbH: 1 (https://510kreport.com/company/eumedics-medizintechnik-und-marketing)
- Leventon, S.A.: 1 (https://510kreport.com/company/leventon)

## Its most-cited devices
- K944900: Therapep (1995), cited by 2
- K961973: DHD Ace with Mask Kit (1996), cited by 1
- K973532: Stealth, Metered Dose Inhaler (Mdi) Spacer Without Integral Actuator (1998), cited by 1
- K926301: Ace Aerosol Enhancer, Hand Held Oral Inhalation CO (1993), cited by 1
- K913326: DHD Metered Dose Inhaler (Mdi) Spacer (1992), cited by 1
- K953206: DHD Metered Dose Inhaler (Mdi) Spacer (Modification) (1995), cited by 1

## Recent decisions
- K973532: Stealth, Metered Dose Inhaler (Mdi) Spacer Without Integral Actuator (Mar 19, 1998)
- K970596: DHD Emerald Product (May 16, 1997)
- K961973: DHD Ace with Mask Kit (Aug 15, 1996)
- K953206: DHD Metered Dose Inhaler (Mdi) Spacer (Modification) (Aug 28, 1995)
- K945118: Expiratory Breathing Exerciser (Jan 13, 1995)
- K944900: Therapep (Jan 6, 1995)
- K926301: Ace Aerosol Enhancer, Hand Held Oral Inhalation CO (Jul 21, 1993)
- K922537: Duralife (Dec 4, 1992)

Source page: https://510kreport.com/company/dhd-diemolding-healthcare-div