FDA applicant

Richards Manufacturer Co.

Mchenry, IL4 decisions1983–19830 recalls

FDA records 4 decisions for Richards Manufacturer Co. (Mchenry, IL) in 1983: 4 510(k) clearances. Most are in product codes JOL (Catheter And Tip, Suction) and JDI (Prosthesis, Hip, Semi-Constrained…). 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, orthopedic panel, where it files most

How often FDA has decided Richards Manufacturer Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richards Manufacturer Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Richards Manufacturer 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 “Richards”

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

Richards Medical Co., Inc. 71

Richards Manufacturer 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 “Richards”