FDA applicant

Spine View, Inc.

Fremont, CA9 decisions2008–20160 recalls

FDA records 9 decisions for Spine View, Inc. (Fremont, CA) from 2008 to 2016: 9 510(k) clearances. Most are in product codes HRX (Arthroscope) and MAX (Intervertebral Fusion Device With Bone Graft…). Its devices cite 21 predicates, 8 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

FIG. A — Illustration, orthopedic panel, where it files most

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

FDA decisions per year

2in 2016

2008high 4 (2012) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

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

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Spine View, Inc.

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?