FDA applicant

Raed M. Ali, M.D., Inc.

Newport Coast, CA2 decisions2019–20210 recalls

FDA records 2 decisions for Raed M. Ali, M.D., Inc. (Newport Coast, CA) from 2019 to 2021: 2 510(k) clearances. All are in product code MAX (Intervertebral Fusion Device With Bone Graft…). 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 Raed M. Ali, M.D., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Raed M. Ali, M.D., Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Raed M. Ali, M.D., Inc.

Which product codes does it file in?

What has FDA decided for it lately?