Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015136935

FEI Number

3015136935

Entity Name

SHENZHEN HANASCO TECHNOLOGY CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

2nd Floor, Building 3, Hualangjia Industrial Park, Kukeng Community, Guanlan Street, Longhua District, Shenzhen Guangdong 518000, CN

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Shenzhen Hanasco Technology Co.,Ltd (Owner Number: 10058766)

Owner / Operator Contact Address

2nd Floor, Building 3, Hualangjia Industrial Park, Kukeng Community, Guanlan Street, Longhua District, Shenzhen, CN-GD 518000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Electric toothbrush (hanasco, huacocare): H1, H2, H3, H6, H7, H8, H9, X1, X6, H3 PLUS, H6 PLUS, H6 ULTRA Mouth Armor/MouthArmor Electric toothbrush: H3 Mouth Armor/MouthArmor Water flosser: H100 Water flosser (hanasco, huacocare):H100 PLUS, H300 PLUS, H600 PLUS, C1 Water flosser (hanasco, huacocare): H100, H200, H300, H400, H500, H600, H700, H800, H900

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2018-10-26
EFS	Unit, Oral Irrigation	Dental	Class 1	872.6510	2018-10-26

Official Correspondent

Hai Li

US Agent Details

FANFEI LIU Email: U.S.agent@frosatechnology.com Phone: (626) 8261385

Related Public Records

Same Entity

Shenzhen Hanasco Technology Co.,Ltd

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
K844318	Pro Pulse, Inc.	ORAL IRRIGATION TIP	1984-11-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015136935. Last updated year: 2026. Please use registration number 3015136935 when referencing this establishment in official correspondence.