FDA applicant

Reznik Instruments

Mchenry, IL9 decisions1981–19810 recalls

FDA records 9 decisions for Reznik Instruments (Mchenry, IL) in 1981: 9 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Reznik Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reznik Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Reznik Instruments

Which product codes does it file in?

What has FDA decided for it lately?