FDA applicant

Ransom and Randolph

Mchenry, IL7 decisions1976–19780 recalls

FDA records 7 decisions for Ransom and Randolph (Mchenry, IL) from 1976 to 1978: 7 510(k) clearances. Most are in product codes EKN (Point, Paper, Endodontic) and EJL (Bur, Dental). 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 Ransom and Randolph’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ransom and Randolph since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ransom and Randolph

Which product codes does it file in?

What has FDA decided for it lately?