# Fossa Medical, Inc.

- Location (FDA's records): Boston, MA
- FDA decisions: 3 (2003–2008): 3 510(k) clearances
- Product codes: FAD (2), EYB (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (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
- Fossa Industries, Inc.: 3 (https://510kreport.com/company/fossa-industries)

## Its most-cited devices
- K031292: Modification to Fossa Ureteral Stone Sweeper (2003), cited by 1
- K033368: Fossa Ureteral Open Lumen Stent (2003), cited by 1

## Recent decisions
- K072293: Fossa Ureteral Open Stents (Aug 6, 2008)
- K033368: Fossa Ureteral Open Lumen Stent (Nov 26, 2003)
- K031292: Modification to Fossa Ureteral Stone Sweeper (May 22, 2003)

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