FDA applicant

Weaver Medical

Salt Lake City, UT1 decision1988–19880 recalls

FDA records 1 decision for Weaver Medical (Salt Lake City, UT) in 1988: 1 510(k) clearance. All are in product code JZT (Fluorometer). 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, immunology panel, where it files most

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

FDA decisions per year

No FDA decision for Weaver Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Weaver”

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

Weaver & Co. 4 Weaver Medical Electronics, Inc. 1

Weaver Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Weaver”