FDA applicant

Activator Methods International, Ltd.

Phoenix, AZ3 decisions2001–20120 recalls

FDA records 3 decisions for Activator Methods International, Ltd. (Phoenix, AZ) from 2001 to 2012: 3 510(k) clearances. All are in product code LXM (Manipulator, Plunger-Like Joint). Its devices cite 3 predicates, 1 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

How often FDA has decided Activator Methods International, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Activator Methods International, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Activator”

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

Activator Methods, Inc. 1

Activator Methods International, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Activator”