FDA applicant

Telectronics and Control Pacing Systems

Englewood, CO1 decision1989–19890 recalls

FDA records 1 decision for Telectronics and Control Pacing Systems (Englewood, CO) in 1989: 1 510(k) clearance. All are in product code 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 Control Pacing Systems’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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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 Cordis Pacing Systems 3

Telectronics and Control Pacing Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Telectronics”