Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010979910

FEI Number

3010979910

Entity Name

IDLIFE, LLC

City/State/Country

Frisco, TX, US

Establishment Address

10825 John W Elliott Dr, Ste 100, Frisco, TX 75033, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device

Owner / Operator

IDLife, LLC (Owner Number: 10085724)

Owner / Operator Contact Address

10825 John W Elliott Dr, Ste 100, Frisco, TX 75033, 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
OIB	Blood And Urine Collection Kit (Excludes Hiv Testing)	Pathology	Class 1	864.3250	2022-07-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

IDLife, LLC

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 3010979910. Last updated year: 2026. Please use registration number 3010979910 when referencing this establishment in official correspondence.