510(k) Report

FDA applicant

Cnmc Co., Inc.

Nashville, TN2 decisions2015–20180 recalls

FDA records 2 decisions for Cnmc Co., Inc. (Nashville, TN) from 2015 to 2018: 2 510(k) clearances. All are in product code IYE (Accelerator, Linear, Medical). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Cnmc Company Incorporated”.

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 Cnmc Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2015: 12018: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Cnmc Co., Inc. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cnmc Co., 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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Which product codes does it file in?

  • IYEAccelerator, Linear, Medical2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K173848Model WP-3840 and WP-3040Cnmc Co., Inc. · 2018
  • K150265Model 206 Electrometer/DosimeterCnmc Company Incorporated · 2015

The one decision as Cnmc Co., Inc. →The one decision as Cnmc Company Incorporated →