FDA applicant

Micromri, Inc.

Langhorne, PA2 decisions2008–20090 recalls

FDA records 2 decisions for Micromri, Inc. (Langhorne, PA) from 2008 to 2009: 2 510(k) clearances. Most are in product codes LLZ (System, Image Processing, Radiological) and MOS (Coil, Magnetic Resonance, Specialty). Its devices cite 3 predicates, 0 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, radiology panel, where it files most

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

FDA decisions per year

1in 2009

2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

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

Planning a device like Micromri, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Micromri, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?