FDA applicant

Rln Systems, Inc.

Jefferson City, MO5 decisions1989–20011 recall

FDA records 5 decisions for Rln Systems, Inc. (Jefferson City, MO) from 1989 to 2001: 5 510(k) clearances. All are in product code ETN (Stimulator, Nerve). 1 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, ear, nose and throat panel, where it files most

How often FDA has decided Rln Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rln Systems, Inc. since 2007.

Recalls per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

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

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Rln Systems, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?