FDA applicant

Transidyne General Corp.

Spartanburg, SC21 decisions1978–19960 recalls

FDA records 21 decisions for Transidyne General Corp. (Spartanburg, SC) from 1978 to 1996: 21 510(k) clearances. Most are in product codes HGW (Sampler, Blood, Fetal) and EGS (Handpiece, Contra- And Right-Angle Attachment…). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Transidyne General Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Transidyne General Corp.

Which product codes does it file in?

What has FDA decided for it lately?