SHENZHEN ZHIQI TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3043626596

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043626596
FEI Number
3043626596
Entity Name
SHENZHEN ZHIQI TECHNOLOGY CO., LTD.
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
B902 38 Qinfu Road, Liuyue Community, Henggang Street, Longgang 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 Zhiqi Technology Co., Ltd. (Owner Number: 10095106)
Owner / Operator Contact Address
B902 38 Qinfu Road, Liuyue Community, Henggang Street, Longgang District, Shenzhen, CN-GD 518000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ULTRASONIC CLEANER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLG Cleaner, Ultrasonic, Medical Instrument General Hospital Class 1 880.6150 2026-01-25

Official Correspondent

No official correspondent registered.

US Agent Details

Bryan Wong Business: PUREVISION AI, INC. (DBA PURE GLOBAL) Email: us-agent@pureglobal.com Phone: (888) 7681688

Related Public Records

Same Entity

Shenzhen Zhiqi Technology Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2025 Young Dental Manufacturing I, LLC 1
BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner, REF PC016, net contents 16 fl. oz., makes 16 gallons of solution.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043626596. Last updated year: 2026. Please use registration number 3043626596 when referencing this establishment in official correspondence.
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