FDA applicant

Kencap, Ltd.

Ringwood, NJ1 decision2001–20010 recalls

FDA records 1 decision for Kencap, Ltd. (Ringwood, NJ) in 2001: 1 510(k) clearance. All are in product code KDD (Kit, Surgical Instrument, 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 Kencap, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kencap, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kencap, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?