# Therex Corp.

- Location (FDA's records): Walpole, MA
- FDA decisions: 26 (1988–1995): 26 510(k) clearances
- Product codes: LJT (24), FMI (1), FPA (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: 20 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K953110: Low Profile Titanium Model Catalog #1003 (Sep 13, 1995)
- K953017: Low Profile Titanium Model Catalog #1003 (Sep 8, 1995)
- K952537: Therex Low Profile Titanium Model 1.0MM I.D./1.8MM O.D. (Jul 6, 1995)
- K950212: A2 Detached Dual Port System (Apr 13, 1995)
- K950131: 1.0MM 1.8MMO.D. Polyurethane Detached Model (Mar 23, 1995)
- K942412: Therex Low-Profile Port - Titanium Model (Aug 19, 1994)
- K936012: Therex Low Profile Port-Titanium Model (Mar 22, 1994)
- K934802: Therex Low-Profile Port-Titanium (Mar 22, 1994)

Source page: https://510kreport.com/company/therex