# Titan Medical, Inc.

- Location (FDA's records): Arden Hills, MN
- FDA decisions: 3 (1987–1988): 3 510(k) clearances
- Product codes: LJT (2), DYB (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
- K875213: Surecath - Itp II Percutaneous Port Access Device (Mar 3, 1988)
- K872149: Surecath-Itp Percutaneous Access Kit (Aug 4, 1987)
- K870542: Vascath Vascular Catheter Placement Kit (Apr 27, 1987)

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