FDA applicant

Nusurg, Inc.

Cincinnati, OH5 decisions1993–19940 recalls

FDA records 5 decisions for Nusurg, Inc. (Cincinnati, OH) from 1993 to 1994: 5 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and KYZ (Syringe, Irrigating (Non Dental)). 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 Nusurg, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nusurg, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Nusurg, Inc.

Which product codes does it file in?

What has FDA decided for it lately?