# Matrix Medica, Inc.

- Location (FDA's records): Orchard Park, NY
- FDA decisions: 14 (1985–1996): 14 510(k) clearances
- Product codes: EIA (2), BTM (1), FYA (1), DRS (1), BZR (1), GDB (1), NAD (1), LRJ (1), BSZ (1), LDD (1), ILI (1), DRL (1)
- Predicates its devices cite: 2 (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
- Microvasive: 1 (https://510kreport.com/company/microvasive)
- Codman & Shurtleff, Inc.: 1 (https://510kreport.com/company/codman-shurtleff)

## Firms that cite its devices most
- O-Two Medical Technologies, Inc.: 1 (https://510kreport.com/company/o-two-medical-technologies)
- Linde Healthcare AB: 1 (https://510kreport.com/company/linde-healthcare)

## Its most-cited devices
- K883833: Nitronox (R), First Response Nitronox (TM) (1989), cited by 2

## Recent decisions
- K961536: Flexscope (Sep 18, 1996)
- K923693: Klorman (Jan 23, 1996)
- K921982: Matrx Hope (R) 5 Resuscitator (Oct 28, 1994)
- K915353: Matrx Medical Maximizer 1000 and 2000 Vacuum Pump (Dec 27, 1991)
- K912661: Matrx, Pyramid Triangle Bandage (Aug 21, 1991)
- K900551: Matrx Disposable Non-Invasive Gelled Pacing Elec. (May 9, 1990)
- K895533: Life Defense Plus (TM), Defibrillator/Monitor/Pacer (Jan 26, 1990)
- K895525: Matrx Battery Charger/Defibrillator Tester (Jan 26, 1990)

Source page: https://510kreport.com/company/matrix-medica