Nuclein, LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3014515702

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014515702
FEI Number
3014515702
Entity Name
Nuclein, LLC
City/State/Country
Austin, TX, US
Establishment Address
8305 Cross Park Dr, Austin, TX 78754, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Nuclein, LLC (Owner Number: 10092415)
Owner / Operator Contact Address
8305 Cross Park Drive, Austin, TX 78754, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

DASH® Negative Control DASH® Rapid PCR Instrument DASH® SARS-CoV-2 & Flu A B Positive Control DASH® SARS-CoV-2 & Flu A/B Test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSU Instrumentation For Clinical Multiplex Test Systems Clinical Chemistry Class 2 862.2570 2025-01-03
QOF Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents Microbiology Class 2 866.3981 2025-01-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nuclein, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3035381641 Nuclein, LLC Austin, TX, US

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2018 Hologic, Inc 2
Panther(R) System, Catalog Number 902615, For Use with Hologic Assays, For In Vitro Diagnostic Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014515702. Last updated year: 2026. Please use registration number 3014515702 when referencing this establishment in official correspondence.
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