FDA applicant

Radiation Development Co., Inc.

Mchenry, IL2 decisions1977–19780 recalls

FDA records 2 decisions for Radiation Development Co., Inc. (Mchenry, IL) from 1977 to 1978: 2 510(k) clearances. All are in product code GDM (Needle, Aspiration And Injection, Reusable). 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 Radiation Development Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Radiation Development Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Radiation Development Co., 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 “Radiation”

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

Radiation Measurements, Inc. 12 Radiation Products Design, Inc. 8 Radiation Technology, Inc. 7 Radiation Oncology Computer Systems 2 Radiation Safety & Nuclear Products, Inc. 2 Radiation Monitoring Devices, Inc. 2 Radiation Products, LLC 1

Radiation Development Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Radiation”