# Dymax Corp

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 7 (1985–2003): 7 510(k) clearances
- Product codes: IYO (4), DQY (2), HGL (1)
- Predicates its devices cite: 4 (4 its own); citations of its devices by later devices: 11 (4 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
- Sonosite,Inc.: 2 (https://510kreport.com/company/sonosite)
- Teratech Corp.: 1 (https://510kreport.com/company/teratech)
- Sheathing Technologies, Inc.: 1 (https://510kreport.com/company/sheathing-technologies)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Inceptio Medical Technologies, LC: 1 (https://510kreport.com/company/inceptio-medical-technologies-lc)
- Bard Access Systems, Inc.: 1 (https://510kreport.com/company/bard-access-systems)

## Its most-cited devices
- K993624: Site-Rite 3 Ultrasound System (1999), cited by 5
- K931403: Siterite Needle Guide (Modified) (1993), cited by 2
- K862127: Dymax Personal Scanner (1986), cited by 2
- K032135: Site-Rite IV Ultrasound System (2003), cited by 1
- K850478: PLUS 1 (1985), cited by 1

## Recent decisions
- K032135: Site-Rite IV Ultrasound System (Jul 21, 2003)
- K993624: Site-Rite 3 Ultrasound System (Nov 10, 1999)
- K931403: Siterite Needle Guide (Modified) (Jul 27, 1993)
- K903158: Siterite Needle Guide (Sep 27, 1990)
- K894415: Dymax Endovaginal Biopsy Guide (Oct 25, 1989)
- K862127: Dymax Personal Scanner (Dec 11, 1986)
- K850478: PLUS 1 (Apr 15, 1985)

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