# Tyrx, Inc.

- Location (FDA's records): Monmouth Junction, NJ
- FDA decisions: 5 (2010–2015): 5 510(k) clearances
- Product codes: FTL (5)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 8 (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
- Tyrx Pharma, Inc.: 3 (https://510kreport.com/company/tyrx-pharma)
- Lifecell Corp.: 1 (https://510kreport.com/company/lifecell)
- Promethean Surgical Devices, Inc.: 1 (https://510kreport.com/company/promethean-surgical-devices)
- Medtronic Tyrx, Inc.: 1 (https://510kreport.com/company/medtronic-tyrx)

## Firms that cite its devices most
- Medtronic Tyrx, Inc.: 2 (https://510kreport.com/company/medtronic-tyrx)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Ariste Medical, LLC: 1 (https://510kreport.com/company/ariste-medical)
- Cormatrix Cardiovascular, Inc.: 1 (https://510kreport.com/company/cormatrix-cardiovascular)

## Its most-cited devices
- K130943: Aigis RX R PM/ Aigis RX R Icd (2013), cited by 3
- K132699: Aigis RX N (Medium), Aigis RX N (Large) (2013), cited by 2
- K093524: Pivit a/B ST and Pivit a/B ST-R (2010), cited by 2
- K131007: Aigis RX N Medium; Aigis RX N Large (2013), cited by 1

## Recent decisions
- K152678: TYRX Neuro Antibacterial Envelope (Nov 17, 2015)
- K132699: Aigis RX N (Medium), Aigis RX N (Large) (Nov 26, 2013)
- K131007: Aigis RX N Medium; Aigis RX N Large (Jul 10, 2013)
- K130943: Aigis RX R PM/ Aigis RX R Icd (May 20, 2013)
- K093524: Pivit a/B ST and Pivit a/B ST-R (Mar 26, 2010)

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