510(k) Report

FDA applicant

Moyco Union Broach, Div., Moyco Technologies, Inc.

York, PA1 decision1996–19960 recalls

FDA records 1 decision for Moyco Union Broach, Div., Moyco Technologies, Inc. (York, PA) in 1996: 1 510(k) clearance. All are in product code LXM (Manipulator, Plunger-Like Joint). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Moyco Union Broach, Div., Moyco Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Moyco Union Broach, Div., Moyco Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Moyco Union Broach, Div., Moyco Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LXMManipulator, Plunger-Like Joint1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K950646IntegratorMoyco Union Broach, Div., Moyco Technologies, Inc. · 19961cites it

What has FDA decided for it lately?

  • K950646IntegratorMoyco Union Broach, Div., Moyco Technologies, Inc. · 1996

The one decision as Moyco Union Broach, Div., Moyco Technologies, Inc. →

Other applicant names beginning “Moyco”

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

Moyco Industries, Inc. 6