FDA applicant

Clark Research and Development, Inc.

Walker, MI2 decisions1984–19960 recalls

FDA records 2 decisions for Clark Research and Development, Inc. (Walker, MI) from 1984 to 1996: 2 510(k) clearances. Most are in product codes IXI (Block, Beam-Shaping, Radiation Therapy) and LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

How often FDA has decided Clark Research and Development, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clark Research and Development, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clark Research and Development, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Clark”

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

Clark Laboratories, Inc. 14 Clark Davis Medical Systems, Inc. 2 Clark Pool & Assoc. 1 Clark Pillow Co., Inc. 1

Clark Research and Development, 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?

Other applicant names beginning “Clark”