FDA applicant

Telectronics and Cordis Pacing Systems

Miami, FL3 decisions1988–19880 recalls

FDA records 3 decisions for Telectronics and Cordis Pacing Systems (Miami, FL) in 1988: 3 510(k) clearances. Most are in product codes DXY (Implantable Pacemaker Pulse-Generator) and DTB (Permanent Pacemaker Electrode). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Telectronics and Cordis Pacing Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Telectronics and Cordis Pacing Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Telectronics and Cordis Pacing Systems by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Telectronics and Cordis Pacing Systems’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Telectronics”

FDA records each applicant name separately; these may or may not be the same firm.

Telectronics, Inc. 108 Telectronics Pacing Systems, Inc. 22 Telectronics and Control Pacing Systems 1

Telectronics and Cordis Pacing Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Telectronics”