510(k) Report

FDA applicant

Easyglide, Ltd.

Bonita Springs, FL5 decisions2009–20120 recalls

FDA records 5 decisions for Easyglide, Ltd. (Bonita Springs, FL) from 2009 to 2012: 5 510(k) clearances. Most are in product codes FDS (Gastroscope And Accessories, Flexible/Rigid) and FDF (Colonoscope And Accessories, Flexible/Rigid). Its devices cite 10 predicates, 5 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

2in 2012

2009: 12010: 22012: 2
2009high 2 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Easyglide, Ltd. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Easyglide, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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