FDA applicant

Nuclear Ent., Ltd.

Mchenry, IL3 decisions1979–19800 recalls

FDA records 3 decisions for Nuclear Ent., Ltd. (Mchenry, IL) from 1979 to 1980: 3 510(k) clearances. All are in product code JJJ (Counter (Beta, Gamma) For Clinical Use). 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, clinical chemistry panel, where it files most

How often FDA has decided Nuclear Ent., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nuclear Ent., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nuclear Ent., Ltd.’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 Data, Inc. 7 Nuclear Medical Systems, Inc. 5 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 Ent., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nuclear”