FDA applicant

Nuclear Data, Inc.

Schaumburg, IL7 decisions1984–19890 recalls

FDA records 7 decisions for Nuclear Data, Inc. (Schaumburg, IL) from 1984 to 1989: 7 510(k) clearances. Most are in product codes KGI (Densitometer, Bone) and IZD (Probe, Uptake, Nuclear). 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 Nuclear Data, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nuclear Data, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Nuclear”

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

Nuclear Medical Laboratories, Inc. 24 Nuclear Diagnostics, Inc. 24 Nuclear Medical Systems, Inc. 5 Nuclear Ent., Ltd. 3 Nuclear Data Systems 2 Nuclear Cardiology Systems, Inc. 2 Nuclear Medicine, Inc. 1 Nuclear Associates 1 Nuclear Concepts, Inc. 1 Nuclear Pacific, Inc. 1 Nuclear Pharmacy, Inc. 1 Nuclear Assoc., Div. Inovision LP 1

Nuclear Data, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nuclear”