FDA applicant

Medic, Inc.

Fremont, NE12 decisions1993–20020 recalls

FDA records 12 decisions for Medic, Inc. (Fremont, NE) from 1993 to 2002: 12 510(k) clearances. Most are in product codes LNH (System, Nuclear Magnetic Resonance Imaging) and MOS (Coil, Magnetic Resonance, Specialty). Its devices cite 1 predicate, 1 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 Medic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medic, 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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Other applicant names beginning “Medic”

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

Medic-Aid, Ltd. 9 Medic Vision - Imaging Solutions, Ltd. 2 Medic Sharplight, Ltd. 1 Medic One 1 Medic Vision Brain Technologies, Ltd. 1 Medic Group of Scandinavia, Inc. 1 Medic Evaluation Devices & Instruments Corp. 1

Medic, Inc.

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 “Medic”