Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030338313

FEI Number

3030338313

Entity Name

GOLDEN HOUR MEDICAL

City/State/Country

Boca Raton, FL, US

Establishment Address

6590 W Rogers Cir Ste 5, Boca Raton, FL 33487, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Golden Hour Medical (Owner Number: 10089810)

Owner / Operator Contact Address

6590 W Rogers Cir., Suite 4, Boca Raton, FL 33487, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ATQ Cuff AutoTQ AeroTQ

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QGX	General Use Pneumatic Tourniquet	General, Plastic Surgery	Class 1	878.5910	2024-01-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Golden Hour Medical

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3007740572	SP MANUFACTURING PTE LTD	Singapore Central Singapore, SG
3005037196	TYNOR ORTHOTICS (P) LTD.	Mohali Punjab, IN
3012360512	VISTAR MEDICAL SUPPLIES CO., LTD.	SHENZHEN Guangdong, CN
3011842549	PT. SP Manufacturing	Batam Riau, ID
3015542886	RING RESCUE INC	Dartmouth Nova Scotia, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030338313. Last updated year: 2026. Please use registration number 3030338313 when referencing this establishment in official correspondence.