FDA applicant

Monadnock Optics, Inc.

Huntingdon Valley, PA1 decision2000–20000 recalls

FDA records 1 decision for Monadnock Optics, Inc. (Huntingdon Valley, PA) in 2000: 1 510(k) clearance. All are in product code GCM (Endoscope, 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Monadnock Optics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Monadnock Optics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?