# Diemolding Corp.

- Location (FDA's records): Canastota, NY
- FDA decisions: 12 (1976–1996): 12 510(k) clearances
- Product codes: BWF (2), CCQ (1), BSK (1), CAN (1), BZA (1), CBD (1), FLN (1), KPQ (1), JDZ (1), BYP (1), CAC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dhd Healthcare Corp.: 2 (https://510kreport.com/company/dhd-healthcare)
- Arm Medical Devices, Inc.: 1 (https://510kreport.com/company/arm-medical-devices)
- Peep Medical, LLC Dba Go2 Devices: 1 (https://510kreport.com/company/peep-medical-dba-go2-devices)

## Its most-cited devices
- K962749: Therapep W/Mouthpiece, W/Pediatric Mask, W/Small Mask, W/Large Mask, Resistor/Port/Mouthpiece, Resistor/Port (1996), cited by 3
- K902114: Cuff-Mate 2 Endotracheal Cuff Inflator & Monitor (1990), cited by 1

## Recent decisions
- K962749: Therapep W/Mouthpiece, W/Pediatric Mask, W/Small Mask, W/Large Mask, Resistor/Port/Mouthpiece, Resistor/Port (Oct 10, 1996)
- K961455: Medshield/Aerochamber (Jul 25, 1996)
- K902713: Access. Kit for the Biosurge Synchronous Autotrans (Jul 25, 1990)
- K902114: Cuff-Mate 2 Endotracheal Cuff Inflator & Monitor (Jul 18, 1990)
- K900754: Respirex 2 (Mar 15, 1990)
- K893791: Breathing Mouthpiece (Jun 23, 1989)
- K781759: Rescal (Nov 27, 1978)
- K780750: O2 Connector (Jul 27, 1978)

Source page: https://510kreport.com/company/diemolding