# Scandius Biomedical, Inc.

- Location (FDA's records): Littleton, MA
- FDA decisions: 6 (2004–2006): 6 510(k) clearances
- Product codes: MAI (2), HWC (2), MBI (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K063497: Modification to Scandius  Tritis Absorbable Tibial Reconstruction System (Dec 19, 2006)
- K063499: Modification to Scandius Tritis Tibial Acl Reconstruction System (Dec 19, 2006)
- K060522: Scandius Tritis Absorbable Tibial Reconstruction System (Apr 11, 2006)
- K052810: Scandius Tritis Tibial Acl Reconstruction System (Dec 20, 2005)
- K041961: Scandius Absorbable Acl Reconstruction System (Oct 20, 2004)
- K041749: Scandius Acl Reconstruction System (Sep 8, 2004)

Source page: https://510kreport.com/company/scandius-biomedical