FDA applicant

Eder Instrument Co, Inc.

Milwaukee, Wi 5320210 decisions1979–19840 recalls

FDA records 10 decisions for Eder Instrument Co, Inc. (Milwaukee, Wi 53202) from 1979 to 1984: 10 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and FET (Endoscopic Video Imaging System/Component…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Eder Instrument Co, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eder Instrument Co, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Eder Instrument Co, Inc.

Which product codes does it file in?

What has FDA decided for it lately?