# Angiotech Medical Device Technologies

- Location (FDA's records): Gainesville
- FDA decisions: 2 (2000–2001): 2 original PMA approvals
- Product codes: PMX (1), NBE (1)
- 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
- P010022: Coseal Surgical Sealant (Coseal) (Dec 14, 2001)
- P990030: Vitagel Surgical Hemostat (Jun 13, 2000)

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