510(k) Report

FDA applicant

Medscope Corp.

Northbrook, IL2 decisions1989–19920 recalls

FDA records 2 decisions for Medscope Corp. (Northbrook, IL) from 1989 to 1992: 2 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and HRX (Arthroscope). 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 Medscope Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medscope Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HETLaparoscope, Gynecologic (And Accessories)1decision
  • HRXArthroscope1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K894303Medscope 4MM ArthroscopeMedscope Corp. · 19891cites it

What has FDA decided for it lately?

  • K903663Medscope 8MM and 10MM LaparoscopeMedscope Corp. · 1992
  • K894303Medscope 4MM ArthroscopeMedscope Corp. · 1989

All 2 as Medscope Corp. →

Other applicant names beginning “Medscope”

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

Medscope Biotech Co., Ltd. 1