FDA applicant

Richard-Allan Medical

Richland, MI8 decisions1991–19940 recalls

FDA records 8 decisions for Richard-Allan Medical (Richland, MI) from 1991 to 1994: 8 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and GEF (Applier, Staple, Surgical,). 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, general and plastic surgery panel, where it files most

How often FDA has decided Richard-Allan Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richard-Allan Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Richard-Allan Medical 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-Allan”

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

Richard Wolf Medical Instruments Corp. 155 Richard'S Medical Equip., Inc. 48 Richard-Allan Medical Ind., Inc. 33 Richard Hamer Assoc., Inc. 8 Richard F. Kronner, M.D. 3 Richard James, Inc. 2 Richard Ting 1 Richard Scott Elliott 1 Richard G. Deniro 1 Richard R. Anthony, M.D. 1 Richard D. Spradlin 1 Richard J. Turner Assoc. 1

Richard-Allan Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Richard-Allan”