FDA applicant

Robin Medical, Inc.

M.P. Misgav, IL2 decisions2004–20110 recalls

FDA records 2 decisions for Robin Medical, Inc. (M.P. Misgav, IL) from 2004 to 2011: 2 510(k) clearances. All are in product code LNH (System, Nuclear Magnetic Resonance Imaging). 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, radiology panel, where it files most

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

FDA decisions per year

1in 2011

2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Robin Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?