# Sontina Medical, LLC

- Location (FDA's records): San Francisco, CA
- FDA decisions: 2 (2012–2014): 2 510(k) clearances
- Product codes: KNW (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 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
- Rubicor Medical, Inc.: 1 (https://510kreport.com/company/rubicor-medical)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K120440: Presto Breast Biopsy Device (2012), cited by 1

## Recent decisions
- K133702: Presto Breast Biopsy Device (Feb 28, 2014)
- K120440: Presto Breast Biopsy Device (May 17, 2012)

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