FDA applicant

Cynergy

Mchenry, IL5 decisions1978–19810 recalls

FDA records 5 decisions for Cynergy (Mchenry, IL) from 1978 to 1981: 5 510(k) clearances. Most are in product codes DTE (Pulse-Generator, Pacemaker, External) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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 Cynergy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cynergy since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cynergy

Which product codes does it file in?

What has FDA decided for it lately?