Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006457763

FEI Number

3006457763

Entity Name

Advance Dx, Inc.

City/State/Country

Scottsdale, AZ, US

Establishment Address

11250 North 118th Way, Scottsdale, AZ 85259, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Advance Dx, Inc. (Owner Number: 9106741)

Owner / Operator Contact Address

11250 North 118th Way, Scottsdale, AZ 85259, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ADVANCEDX 100 SERUM SEPARATOR

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	2007-09-06

Official Correspondent

Ned Bedrio

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Advance Dx, 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 3006457763. Last updated year: 2026. Please use registration number 3006457763 when referencing this establishment in official correspondence.