FDA applicant

Cmf Medicon Surgical, Inc.

Jacksonville, FL4 decisions2019–20240 recalls

FDA records 4 decisions for Cmf Medicon Surgical, Inc. (Jacksonville, FL) from 2019 to 2024: 4 510(k) clearances. Most are in product codes NKB (Thoracolumbosacral Pedicle Screw System) and PLR (Spinal Vertebral Body Replacement Device -…). Its devices cite 7 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, orthopedic panel, where it files most

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

FDA decisions per year

2in 2024

2019high 2 (2024) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Cmf Medicon Surgical, Inc. by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Cmf Medicon Surgical, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?