# Dynarad Corp.

- Location (FDA's records): Deer Park, NY
- FDA decisions: 9 (1993–2000): 9 510(k) clearances
- Product codes: IZL (5), IZX (1), ITY (1), EHD (1), IZH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Portavision Medical, LLC: 1 (https://510kreport.com/company/portavision-medical)
- Philips Medical Systems (Cleveland), Inc.: 1 (https://510kreport.com/company/philips-medical-systems-cleveland)

## Its most-cited devices
- K981267: Facts Monoblock (1998), cited by 1
- K973833: Control, X-Ray Diagnostic, Generator, High Voltage, Assembly, Tube Housing Diagnostic, Beam Limiting Device, Manual (1997), cited by 1

## Recent decisions
- K000052: X-Ray Monoblock, Monoblock XRS-60-330 (Feb 10, 2000)
- K981267: Facts Monoblock (May 6, 1998)
- K973833: Control, X-Ray Diagnostic, Generator, High Voltage, Assembly, Tube Housing Diagnostic, Beam Limiting Device, Manual (Dec 30, 1997)
- K932356: Nova XM2 (Feb 8, 1995)
- K941363: Phantom (Jul 20, 1994)
- K932353: HF-110A (Jan 31, 1994)
- K932355: 9150A, 1100F (Aug 3, 1993)
- K932354: 9170, 1170 (Jul 23, 1993)

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