510(k) Report

FDA applicant

Nbs Products CO

New Brunswick, NJ1 decision2000–20001 recall

FDA records 1 decision for Nbs Products CO (New Brunswick, NJ) in 2000: 1 510(k) clearance. All are in product code HIF (Insufflator, Laparoscopic). 1 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 Nbs Products CO’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nbs Products CO since 2007.

Recalls per year

1in 2024

2024: 1
2007high 1 (2024) · low 0 (2007)2026

Class I Class II/III not classified

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

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