510(k) Report

FDA applicant

Endoscopic Surgical Products, Inc.

Minnetonka, MN2 decisions1992–19940 recalls

FDA records 2 decisions for Endoscopic Surgical Products, Inc. (Minnetonka, MN) from 1992 to 1994: 2 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and GCJ (Laparoscope, General & Plastic Surgery). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Endoscopic Surgical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Endoscopic Surgical Products, 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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Which product codes does it file in?

  • HETLaparoscope, Gynecologic (And Accessories)1decision
  • GCJLaparoscope, General & Plastic Surgery1decision

What has FDA decided for it lately?

  • K921335Ultraflow Suction-Irrigation CannulaEndoscopic Surgical Products, Inc. · 1994
  • K921336Trocar Grasper/Anvil ApproximatorEndoscopic Surgical Products, Inc. · 1992

All 2 as Endoscopic Surgical Products, Inc. →

Other applicant names beginning “Endoscopic”

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

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