510(k) Report

FDA applicant

Endoscopic Surgical Accessories, Inc.

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Endoscopic Surgical Accessories, Inc. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code KNS (Unit, Electrosurgical, Endoscopic (With Or…). 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 Endoscopic Surgical Accessories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endoscopic Surgical Accessories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Endoscopic Surgical Accessories, Inc.’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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Other applicant names beginning “Endoscopic”

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