FDA applicant

Symex Corp.

Tulsa, OK1 decision1994–19940 recalls

FDA records 1 decision for Symex Corp. (Tulsa, OK) in 1994: 1 510(k) clearance. All are in product code GQP (Antisera, Neutralization, Parainfluenza Virus…). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Symex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Symex Corp.

Which product codes does it file in?

What has FDA decided for it lately?