510(k) Report

FDA applicant

Cemco Tool Co., Inc.

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Cemco Tool Co., Inc. (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code EKP (Reamer, Pulp Canal, Endodontic). 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, dental panel, where it files most

How often FDA has decided Cemco Tool Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cemco Tool Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cemco Tool 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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Other applicant names beginning “Cemco”

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