510(k) Report

FDA applicant

Master Benefits, Inc.

Hayward, CA1 decision2001–20010 recalls

FDA records 1 decision for Master Benefits, Inc. (Hayward, CA) in 2001: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Master Benefits, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision

What has FDA decided for it lately?

  • K003521Dispo-Med 7.6 Liter Sharps ContainerMaster Benefits, Inc. · 2001

The one decision as Master Benefits, Inc. →

Other applicant names beginning “Master”

FDA records each applicant name separately; these may or may not be the same firm.

The Master Medical Corp. 6Master & Frank Enterprses Co., Ltd. 1Master & Frank Enterprise Co., Ltd. 1Master Hydro Systems, Inc. 1Master Medical Services, Inc. 1Master & Frank Ent. Co., Ltd. 1