Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027520354

FEI Number

3027520354

Entity Name

Hansfive (Hangzhou) Dental Technology Co.,Ltd

City/State/Country

Hangzhou city Zhejiang, CN

Establishment Address

Buildinhg 2, No. 5 Yichuang Road, Yuhang Street, Yuhang District, Hangzhou, Zhejiang, China, Floor 3, Building 2, No.7, Yuda Road, Yuhang Street, Yuhang District, Hangzhou, Zhejiang, China, Hangzhou city Zhejiang 311100, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Hansfive (Hangzhou) Dental Technology Co., Ltd. (Owner Number: 10088065)

Owner / Operator Contact Address

17th Floor, No. 1199, West Wenyi Rd, Hangzhou city, CN-ZJ 311100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Buccal Tubes Crimpable Hook Lingual Button Nickel Titanium Root Canal File Orthodontic Plier Orthodontic Spring

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DZD	Tube, Orthodontic	Dental	Class 1	872.5410	2025-12-14
ECN	Clamp, Wire, Orthodontic	Dental	Class 1	872.5410	2025-12-15
EKS	File, Pulp Canal, Endodontic	Dental	Class 1	872.4565	2025-12-15
JEX	Plier, Orthodontic	Dental	Class 1	872.4565	2026-02-03
ECO	Spring, Orthodontic	Dental	Class 1	872.5410	2025-12-14

Official Correspondent

Lihong Qin

US Agent Details

XUEHAI SHAO Business: VITANG TECHNOLOGY,LLC Email: regrek.cs@hotmail.com Phone: (773) 2367691

Related Public Records

Same Entity

Hansfive (Hangzhou) Dental 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
K864976	Endo Technic Corp.	SOLUSET CALCIUM DEMINERALIZING SOLUTION	1987-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027520354. Last updated year: 2026. Please use registration number 3027520354 when referencing this establishment in official correspondence.