# Kent Medical Devices, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: NEU (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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
- Cytophil, Inc.: 1 (https://510kreport.com/company/cytophil)
- Carbon Medical Technologies, Inc.: 1 (https://510kreport.com/company/carbon-medical-technologies)

## Firms that cite its devices most
- Scion Medical Technologies, LLC: 2 (https://510kreport.com/company/scion-medical-technologies)
- Breast-Med, Inc.: 1 (https://510kreport.com/company/breast-med)
- Cendres & Metaux SA: 1 (https://510kreport.com/company/cendres-metaux)

## Its most-cited devices
- K093473: KMD-MARK1 Tissue Marker (2010), cited by 4

## Recent decisions
- K093473: KMD-MARK1 Tissue Marker (Jul 2, 2010)

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