# Miromatrix Medical, Inc.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 6 (2014–2017): 6 510(k) clearances
- Product codes: FTM (2), KGN (2), OXH (2)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 6 (3 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
- Cook Biotech, Inc.: 2 (https://510kreport.com/company/cook-biotech)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)

## Firms that cite its devices most
- Tybr Health: 1 (https://510kreport.com/company/tybr-health)
- Reprise Biomedical, Inc.: 1 (https://510kreport.com/company/reprise-biomedical)
- Geistlich Pharma AG: 1 (https://510kreport.com/company/geistlich-pharma)

## Its most-cited devices
- K140510: Miromatrix Wound Matrix (2014), cited by 3
- K134033: Miromatrix Biological Mesh (2014), cited by 1
- K162570: Miromatrix Biological Mesh TW (2017), cited by 1
- K150341: Miromatrix Biological Mesh RS (2015), cited by 1

## Recent decisions
- K162570: Miromatrix Biological Mesh TW (Feb 16, 2017)
- K160400: Miromatrix Biological Mesh (Jun 8, 2016)
- K150341: Miromatrix Biological Mesh RS (May 12, 2015)
- K143426: Wound Matrix TF (Jan 27, 2015)
- K140510: Miromatrix Wound Matrix (Jun 19, 2014)
- K134033: Miromatrix Biological Mesh (Mar 31, 2014)

Source page: https://510kreport.com/company/miromatrix-medical