Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013756523

FEI Number

3013756523

Entity Name

APEX BIOLOGIX

City/State/Country

W Bountiful, UT, US

Establishment Address

2561 S 1560 W, Suite B, W Bountiful, UT 84087, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Apex Biologix (Owner Number: 10055369)

Owner / Operator Contact Address

2561 S 1560 W, Suite B, Woods Cross, UT 84087, US

Initial Importer Flag

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
JJH	Clinical Sample Concentrator	Clinical Chemistry	Class 1	862.2310	2022-11-14
JQC	Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use	Clinical Chemistry	Class 1	862.2050	2018-08-25

Official Correspondent

Brent Bowman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Apex Biologix

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 3013756523. Last updated year: 2026. Please use registration number 3013756523 when referencing this establishment in official correspondence.