FDA applicant

Technicare Corp.

Solon, OH32 decisions1980–19850 recalls

FDA records 32 decisions for Technicare Corp. (Solon, OH) from 1980 to 1985: 32 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and JAK (System, X-Ray, Tomography, Computed). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Technicare Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Technicare Corp.

Which product codes does it file in?

What has FDA decided for it lately?