FDA applicant

Xpandortho, Inc.

La Jolla, CA1 decision2017–20170 recalls

FDA records 1 decision for Xpandortho, Inc. (La Jolla, CA) in 2017: 1 510(k) clearance. All are in product code ONN (Intraoperative Orthopedic Joint Assessment Aid). 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, neurology panel, where it files most

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

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Xpandortho, Inc. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Xpandortho, Inc.

Which product codes does it file in?

What has FDA decided for it lately?