FDA applicant

Alter-G, Inc.

Menlo Park, CA1 decision2008–20081 recall

FDA records 1 decision for Alter-G, Inc. (Menlo Park, CA) in 2008: 1 510(k) clearance. All are in product code BXB (Exerciser, Powered). 1 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 Alter-G, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

1in 2011

2008high 1 (2011) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Alter-G, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Alter-G, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?