# Cordis Leads, Inc.

- Location (FDA's records): Suffield, CT
- FDA decisions: 4 (1988–1988): 4 510(k) clearances
- Product codes: DTB (3), LDF (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
- K883070: Encor Unipolar VS-1 Leads (Dec 5, 1988)
- K873772: Changes to Encor Pervenous J-Atrial Leads (Oct 19, 1988)
- K882045: High Torque Temporary Pervenous Lead W/Depth Mark (Jul 12, 1988)
- K874366: Encor Bipolar Act/Fixa Lead W/Por Sur Ele #329-201 (Jun 16, 1988)

Source page: https://510kreport.com/company/cordis-leads