Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027225088

FEI Number

3027225088

Entity Name

STARLING MEDICAL

City/State/Country

Houston, TX, US

Establishment Address

2450 Holcombe Blvd Ste 1320, Houston, TX 77021, US

Establishment Type(s)

Manufacture Medical Device,Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Starling Medical (Owner Number: 10087865)

Owner / Operator Contact Address

2450 Holcombe Boulevard, Suite 1320, Houston, TX 77021, 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
KQO	Automated Urinalysis System	Clinical Chemistry	Class 1	862.2900	2025-08-13

Official Correspondent

Hannah McKenney

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Starling Medical

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K101852	Iris International Inc., A Division of Iris Iris I	CHEM VELOCITY AUTOMATED URINE CHEMISTRY SYSTEM, STRIPS AND CALCHEK KIT	2011-03-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027225088. Last updated year: 2026. Please use registration number 3027225088 when referencing this establishment in official correspondence.