FDA applicant

Syntex Corp.

Mchenry, IL10 decisions1976–19920 recalls

FDA records 10 decisions for Syntex Corp. (Mchenry, IL) from 1976 to 1992: 10 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and EJJ (Alloy, Amalgam). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Syntex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Syntex”

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

Syntex Healthcare Products Co., Ltd. 17 Syntex Dental Products, Inc. 3

Syntex Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Syntex”