DXTERITY DIAGNOSTICS INC.

FDA Device Registration & Listing · Torrance, CA, US · Registration 3009870369

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
3009870369
FEI Number
3009870369
Entity Name
DXTERITY DIAGNOSTICS INC.
City/State/Country
Torrance, CA, US
Establishment Address
2441 W. 205th St. Suite C100, Torrance, CA 90501, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
DxTerity Diagnostics Inc. (Owner Number: 10080900)
Owner / Operator Contact Address
2441 W. 205th St. Suite C100, Torrance, CA 90501, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNK Container, Specimen Mailer And Storage, Non-Sterile Pathology Class 1 864.3250 2021-03-04
PPM General Purpose Reagent Pathology Class 1 864.4010 2022-03-02

Official Correspondent

Robert Terbrueggen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DxTerity Diagnostics Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009870369. Last updated year: 2026. Please use registration number 3009870369 when referencing this establishment in official correspondence.
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