Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012074930

FEI Number

3012074930

Entity Name

HEARTLAND TECHNOLOGY DONGGUAN CO.,LTD.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Room 301,Building2,NO.24,Binhe Road Zhangmutou,Zhangmutou Town,Dongguan City,Guangdong Province,China, Dongguan Guangdong 523626, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Heartland Technology Dongguan Co.,Ltd. (Owner Number: 10090404)

Owner / Operator Contact Address

Room 301,Building2,NO.24,Binhe Road Zhangmutou,Zhangmutou Town,Dongguan City,Guangdong Province,China, Dongguan, CN-GD 523626, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bloom Pod Menstrual cup FP-240002

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXQ	Vibrator For Therapeutic Use, Genital	Obstetrics/Gynecology	Class 2	884.5960	2024-03-24
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2024-05-05

Official Correspondent

Shenglan Yu

US Agent Details

Thomas Anderson Business: AZUR US Limited Email: AmbertFDA@outlook.com Phone: (303) 4370886

Related Public Records

Same Entity

Heartland Technology Dongguan Co.,Ltd.

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 3012074930. Last updated year: 2026. Please use registration number 3012074930 when referencing this establishment in official correspondence.