# Scion Medical Technologies, LLC

- Location (FDA's records): Newtown Square, PA
- FDA decisions: 6 (2013–2017): 6 510(k) clearances
- Product codes: NEU (4), KNW (2)
- Predicates its devices cite: 10 (4 its own); citations of its devices by later devices: 6 (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 whose devices it cites most
- Kent Medical Devices, Inc.: 2 (https://510kreport.com/company/kent-medical-devices)
- Carbon Medical Technologies, Inc.: 2 (https://510kreport.com/company/carbon-medical-technologies)
- Sanarus Medical, Inc.: 1 (https://510kreport.com/company/sanarus-medical)
- Senorx, Inc.: 1 (https://510kreport.com/company/senorx)

## Firms that cite its devices most
- Surgmark GmbH: 1 (https://510kreport.com/company/surgmark)
- Viscus Biologics, LLC: 1 (https://510kreport.com/company/viscus-biologics)

## Its most-cited devices
- K140835: General and Plastic Surgery (2014), cited by 3
- K130763: Beacon Tissue Marker (2013), cited by 2
- K123606: Cassi II Rotational Core Biopsy System; Cassi Quadpoint Disposable (2013), cited by 1

## Recent decisions
- K170905: Star Tissue Marker (Apr 27, 2017)
- K161234: CASSI II Rotational Core Biopsy System (Aug 3, 2016)
- K153189: Beacon Tissue Marker (SE) (Dec 17, 2015)
- K140835: General and Plastic Surgery (May 20, 2014)
- K130763: Beacon Tissue Marker (May 8, 2013)
- K123606: Cassi II Rotational Core Biopsy System; Cassi Quadpoint Disposable (Mar 1, 2013)

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