FDA applicant

Ritter Co.

Mchenry, IL10 decisions1976–19830 recalls

FDA records 10 decisions for Ritter Co. (Mchenry, IL) from 1976 to 1983: 10 510(k) clearances. Most are in product codes KLC (Chair, Dental, With Operative Unit) and DXN (System, Measurement, Blood-Pressure…). 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 Ritter Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ritter Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ritter”

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

Ritter Implants GmbH & Co. KG 3 Ritter Concept GmbH 1

Ritter Co.

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?

Other applicant names beginning “Ritter”