FDA applicant

The Synaptic Corp.

Aurora, CO1 decision1997–19970 recalls

FDA records 1 decision for The Synaptic Corp. (Aurora, CO) in 1997: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for The Synaptic Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Synaptic 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 “The”

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

Synaptic Medical Corporation 7

The Synaptic Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”