Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027388179

FEI Number

3015342436

Entity Name

Zeo Scientifix Inc.

City/State/Country

Fort Lauderdale, FL, US

Establishment Address

3300 S. University Drive, Suite 246, Fort Lauderdale, FL 33328, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Zeo Scientifix Inc. (Owner Number: 10088106)

Owner / Operator Contact Address

3300 S. University Drive, Suite 246, Fort Lauderdale, FL 33328, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Patient Pure X-PPX Collection Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PQD	Blood Specimen Collection Convenience Kit (Excludes Hiv)	Clinical Chemistry	Class 2	862.1675	2023-05-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Zeo Scientifix 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 3027388179. Last updated year: 2026. Please use registration number 3027388179 when referencing this establishment in official correspondence.