FDA applicant

J-Lloyd Medical, Inc.

West Berlin, NJ16 decisions1993–19980 recalls

FDA records 16 decisions for J-Lloyd Medical, Inc. (West Berlin, NJ) from 1993 to 1998: 16 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and DYG (Catheter, Flow Directed). Its devices cite 5 predicates, 5 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, cardiovascular panel, where it files most

How often FDA has decided J-Lloyd Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for J-Lloyd Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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J-Lloyd Medical, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?