FDA applicant

Zinetics Medical, Inc.

Salt Lake City, UT4 decisions1988–19940 recalls

FDA records 4 decisions for Zinetics Medical, Inc. (Salt Lake City, UT) from 1988 to 1994: 4 510(k) clearances. Most are in product codes KLA (Monitor, Esophageal Motility, Anorectal…) and FFT (Electrode, Ph, Stomach). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Zinetics Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zinetics Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Zinetics”

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

Zinetics Medical Technology Corp. 1

Zinetics Medical, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Zinetics”