# Tpl-Cordis, Inc.

- Location (FDA's records): Suffield, CT
- FDA decisions: 6 (1987–1989): 6 510(k) clearances
- Product codes: DXY (4), DTB (1), KRG (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
- K885240: Modified Ancor & HI-Flex Unipolar Active Fix. Lead (Feb 10, 1989)
- K882429: Model 255A Programmer Iii, W/Software Revi. 4004 (Jul 22, 1988)
- K880898: Multicor and Pacemakers (May 6, 1988)
- K880432: Vicor Pacer, Model 410A (Feb 22, 1988)
- K873158: Modified Multicor and Omni-Stanicor Pacemakers (Jan 7, 1988)
- K873202: Vicor, Model 410A (Oct 15, 1987)

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