FDA applicant

Dhason Brothers, Inc.

Hyattsville, MD14 decisions1989–19890 recalls

FDA records 14 decisions for Dhason Brothers, Inc. (Hyattsville, MD) in 1989: 14 510(k) clearances. Most are in product codes LXH (Orthopedic Manual Surgical Instrument) and LRW (Scissors, General, Surgical). 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, orthopedic panel, where it files most

How often FDA has decided Dhason Brothers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dhason Brothers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dhason Brothers, Inc.

Which product codes does it file in?

What has FDA decided for it lately?