FDA applicant

Rinn Corp.

Elgin, IL5 decisions1978–19930 recalls

FDA records 5 decisions for Rinn Corp. (Elgin, IL) from 1978 to 1993: 5 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and EGZ (Holder, Film, X-Ray). 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, radiology panel, where it files most

How often FDA has decided Rinn Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rinn Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Rinn”

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

Rinn Dental Products 1

Rinn Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rinn”