# Dilon Technologies, Inc.

- Location (FDA's records): Newport News, VA
- FDA decisions: 4 (1999–2017): 3 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Dilon Technologies, Inc. (3); Dilon Technologies, LLC (1)
- Product codes: IYX (3), PMX (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (2 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
- Adac Laboratories: 1 (https://510kreport.com/company/adac-laboratories)
- Digirad Corp.: 1 (https://510kreport.com/company/digirad)

## Firms that cite its devices most
- GE Healthcare: 1 (https://510kreport.com/company/ge-healthcare)

## Its most-cited devices
- K984466: Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5 (1999), cited by 2
- K082588: Gammaloc System, Model 03-00001 (2009), cited by 1

## Recent decisions
- P170012: HEMOBLAST™ Bellows (Dec 15, 2017)
- K110384: Dilon 6800 Acella (Acella) (May 3, 2011)
- K082588: Gammaloc System, Model 03-00001 (Dec 11, 2009)
- K984466: Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5 (Mar 16, 1999)

Source page: https://510kreport.com/company/dilon-technologies