FDA applicant

Janneck Ent. of Texas

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Janneck Ent. of Texas (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 Janneck Ent. of Texas’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Janneck Ent. of Texas since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Janneck Ent. of Texas

Which product codes does it file in?

What has FDA decided for it lately?