FDA applicant

U.S. Safety Syringes Co., Inc.

Crofton, MD7 decisions2000–20090 recalls

FDA records 7 decisions for U.S. Safety Syringes Co., Inc. (Crofton, MD) from 2000 to 2009: 7 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and FPA (Set, Administration, Intravascular). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 U.S. Safety Syringes Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2009

2007high 3 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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U.S. Safety Syringes Co., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?