510(k) Report

FDA applicant

Nv Cormed

Oviedo, FL1 decision2005–20050 recalls

FDA records 1 decision for Nv Cormed (Oviedo, FL) in 2005: 1 510(k) clearance. All are in product code MNH (Orthosis, Spondylolisthesis Spinal Fixation). 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 Nv Cormed’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nv Cormed since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • MNHOrthosis, Spondylolisthesis Spinal Fixation1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K051959NV Cormed Solas Spinal SystemNv Cormed · 20051cites it

What has FDA decided for it lately?

  • K051959NV Cormed Solas Spinal SystemNv Cormed · 2005

The one decision as Nv Cormed →