FDA applicant

Sanyo North America Corp.

Tasca, IL1 decision2001–20010 recalls

FDA records 1 decision for Sanyo North America Corp. (Tasca, IL) in 2001: 1 510(k) clearance. All are in product code MQG (Accessory, Assisted Reproduction). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Sanyo North America Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sanyo North America 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 “Sanyo”

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

Sanyo Electric, Inc. 3

Sanyo North America Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Sanyo”