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Nuclear Diagnostics, Inc.

US

Last updated May 23, 2026

What Nuclear Diagnostics, Inc. makes

Nuclear Diagnostics, Inc. manufactures in vitro diagnostic test kits and radioimmunoassay kits, including the STIKSEP-T4 RIA KIT, SERUM THYROTROPIN ASSAY KIT, NUCLIPASE (I125) PANCREATIC LIPASE, and other thyroid and pancreatic function tests. Their products also include enzyme immunoassays, radioassays, and quality control materials like the TRI-LEVEL NDI CONTROL.

The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry. Nuclear Diagnostics, Inc. is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Nuclear Diagnostics, Inc. manufacture?

Nuclear Diagnostics, Inc. manufactures in vitro diagnostic test kits and radioimmunoassay kits, including thyroid and pancreatic function tests, enzyme immunoassays, radioassays, and quality control materials.

Where is Nuclear Diagnostics, Inc. based?

Nuclear Diagnostics, Inc. is based in the United States, as indicated by the country information provided in the device data.

Which regulatory registries list Nuclear Diagnostics, Inc.'s devices?

Nuclear Diagnostics, Inc.'s devices are listed in the FDA 510(k) registry, which is the only registry mentioned in the provided device data.

How are Nuclear Diagnostics, Inc.'s devices classified?

Nuclear Diagnostics, Inc.'s devices are classified as Class I and Class II, which are medical device classifications that determine the level of regulatory control required.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
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Catalogue (27)

DeviceModel / ReferenceRegistriesClassStatus
Technologist Choice TOR-23BT
FDA UDI
Class IActive
Saturo URC-120Y
FDA UDI
Class IActive
Stiksep-T4 Ria Kit K780423
FDA 510(k)
Class IIActive
Serum Thyrotropin Assay Kit, Tipsep- K833713
FDA 510(k)
Class IIActive
Nuclipase (i125) Pancreatic Lipase K823860
FDA 510(k)
Class IActive
Hermes Hd Aq Acquisition Station And Hermes Workstation K002782
FDA 510(k)
Class IIActive
Bio Nuclear Diagnostics (endo)cervical Sampler For Gyn Cytology K081522
FDA 510(k)
Class IIActive
Stiksep-T3 Kit K780486
FDA 510(k)
Class IIActive
Radioassay For Total Serum Thyroxine K780644
FDA 510(k)
Class IIActive
Tipsep-Tbg Assay K861735
FDA 510(k)
Class IIActive
Elipase Human Pancreatic Lipase Enzymeimmunoassay K923917
FDA 510(k)
Class IActive
Tipsep Digoxin Ria K852291
FDA 510(k)
Class IIActive
Tri-Level Ndi Control K810906
FDA 510(k)
Class IActive
Tipsep-T3u Triiodothyronine Uptake K792484
FDA 510(k)
Class IIActive
Nucli-Pap Tm-(i125)-Pap Radioimmunoas- K802886
FDA 510(k)
Class IIActive
Nuclitryp(tm)(i125)-Human Pancrea Cath Try Rad Kit K932406
FDA 510(k)
Class IActive
Nuclear Laser Alignment System For Cardic Stress K860472
FDA 510(k)
Class IActive
Tipsep-Cortisol Ria Diagnostic Kit K872177
FDA 510(k)
Class IIActive
Spinsep-T3 K771854
FDA 510(k)
Class IIActive
Ria Diag. Test Kit For Indexing Thyrox. K781560
FDA 510(k)
Class IIActive
Hermes Hdaq Acquisition Station And Hermes Workstation, Ver. 3.4 K021656
FDA 510(k)
Class IIActive
Tria-Peg Ria Diag. Kit K780292
FDA 510(k)
Class IIActive
Spinsep-Fe59 K790133
FDA 510(k)
Class IActive
Tsh-P.e.g. K811558
FDA 510(k)
Class IIActive
Enzlipase, Enzymatic Lipase Kit K862312
FDA 510(k)
Class IActive
Spinsep-Tbg K771341
FDA 510(k)
Class IIActive
Tipsep-T4(ria) T4 Radioimmunoassay K792599
FDA 510(k)
Class IIActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Bio Nuclear Diagnostics, Inc. TORONTO Ontario · CA FEI 3005892511