FDA applicant

Nuclear Assoc., Div. Inovision LP

Carle Place, NY1 decision2001–20010 recalls

FDA records 1 decision for Nuclear Assoc., Div. Inovision LP (Carle Place, NY) in 2001: 1 510(k) clearance. All are in product code KPT (Calibrator, Dose, Radionuclide). 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 Assoc., Div. Inovision LP’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nuclear Assoc., Div. Inovision LP since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 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

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nuclear”