FDA applicant

Endoscopic Innovations, Inc.

Morris, MN1 decision1994–19940 recalls

FDA records 1 decision for Endoscopic Innovations, Inc. (Morris, MN) in 1994: 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 Innovations, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endoscopic Innovations, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Endoscopic”

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

Endoscopic Technologies, Inc. 8 Endoscopic Technologies, Inc. D/B/A Estech 5 Endoscopic Concepts, Inc. 4 Endoscopic Surgical Products, Inc. 2 Endoscopic Surgical Accessories, Inc. 1

Endoscopic Innovations, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Endoscopic”