FDA applicant

Lunar Radiation Corp.

Mchenry, IL6 decisions1980–19881 recall

FDA records 6 decisions for Lunar Radiation Corp. (Mchenry, IL) from 1980 to 1988: 6 510(k) clearances. Most are in product codes KGI (Densitometer, Bone) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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, radiology panel, where it files most

How often FDA has decided Lunar Radiation Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lunar Radiation Corp. since 2007.

Recalls per year

1in 2018

2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Lunar Radiation Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Lunar”

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

Lunar Corp. 29

Lunar Radiation Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Lunar”