FDA applicant

The Jarid Group, Inc.

Wayside, NJ3 decisions1987–19870 recalls

FDA records 3 decisions for The Jarid Group, Inc. (Wayside, NJ) in 1987: 3 510(k) clearances. Most are in product codes LRO (General Surgery Tray) and LRS (I.V. Start Kit). 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 The Jarid Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Jarid Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Jarid Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?