# Diacor, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 10 (1986–2013): 10 510(k) clearances
- Product codes: IWE (4), IYE (4), FRZ (1), IXI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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 whose devices it cites most
- Orfit Industries NV: 1 (https://510kreport.com/company/orfit-industries)

## Firms that cite its devices most
- Qfix: 1 (https://510kreport.com/company/qfix)
- Gammex, Inc.: 1 (https://510kreport.com/company/gammex)

## Its most-cited devices
- K872489: Centralite (1987), cited by 1
- K121929: Zephyr 'X-Series Patient Transfer Sled (2013), cited by 1

## Recent decisions
- K121929: Zephyr 'X-Series Patient Transfer Sled (Jan 17, 2013)
- K050888: Integra Immobilization System (May 23, 2005)
- K954414: Centralite Backpointer (Oct 23, 1995)
- K953046: Peri-Pusher (Sep 22, 1995)
- K950112: Centralite (R)-DLL Series (Aug 16, 1995)
- K934566: Radassist (Nov 3, 1993)
- K930246: Mammorx (Jul 26, 1993)
- K893398: Centralite Backpointer (Aug 17, 1989)

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