FDA applicant

Inner Vision Mri, Ltd.

Teaneck, NJ1 decision1996–19960 recalls

FDA records 1 decision for Inner Vision Mri, Ltd. (Teaneck, NJ) in 1996: 1 510(k) clearance. 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 Inner Vision Mri, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inner Vision Mri, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inner Vision Mri, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Inner”

FDA records each applicant name separately; these may or may not be the same firm.

Inner Mongolia Cureguard Medical Technology Co., Ltd. 3 Inner Mongolia Boming Medical Supplies Co., Ltd. 2 Inner Vision Biometrics Pty, Ltd. 1 Inner Act, LLC 1 Inner Mongolia Cureguard Medical Materials Co., Ltd. 1

Inner Vision Mri, Ltd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Inner”