FDA applicant

Rose KG

Washington, DC1 decision1985–19850 recalls

FDA records 1 decision for Rose KG (Washington, DC) in 1985: 1 510(k) clearance. All are in product code GAA (Needle, Aspiration And Injection, Disposable). 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 Rose KG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rose KG since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Rose”

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

Rose K International, Ltd. 2

Rose KG

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rose”