510(k) Report

FDA applicant

Richard'S Medical Equip., Inc.

Mchenry, IL48 decisions1976–19831 recall

FDA records 48 decisions for Richard'S Medical Equip., Inc. (Mchenry, IL) from 1976 to 1983: 48 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and ETB (Prosthesis, Partial Ossicular Replacement). 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, orthopedic panel, where it files most

How often FDA has decided Richard'S Medical Equip., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richard'S Medical Equip., Inc. since 2007.

Recalls per year

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Richard'S Medical Equip., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Richard'S”

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