FDA applicant

Machida America, Inc.

Mchenry, IL8 decisions1981–19880 recalls

FDA records 8 decisions for Machida America, Inc. (Mchenry, IL) from 1981 to 1988: 8 510(k) clearances. Most are in product codes EQN (Laryngoscope, Nasopharyngoscope) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, ear, nose and throat panel, where it files most

How often FDA has decided Machida America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Machida America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Machida”

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

Machida, Inc. 1 Machida Endoscope Co., Ltd. 1

Machida America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Machida”