FDA applicant

Medical Device Advisory Development Group

Irvine, CA1 decision2005–20050 recalls

FDA records 1 decision for Medical Device Advisory Development Group (Irvine, CA) in 2005: 1 510(k) clearance. All are in product code MNH (Orthosis, Spondylolisthesis Spinal Fixation). 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 Medical Device Advisory Development Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Device Advisory Development Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Device Advisory Development Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Medical Device Advisory Development Group

Which product codes does it file in?

What has FDA decided for it lately?