FDA applicant

Jace Systems, Inc.

Moorestown, NJ6 decisions1992–19940 recalls

FDA records 6 decisions for Jace Systems, Inc. (Moorestown, NJ) from 1992 to 1994: 6 510(k) clearances. Most are in product codes BXB (Exerciser, Powered) and JFA (Exerciser, Finger, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Jace Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Jace”

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

Jace Medical, LLC 2

Jace Systems, 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?

Other applicant names beginning “Jace”