SHANGHAI SHIFT ELECTRICS CO.,LTD.

FDA Device Registration & Listing · SHANGHAI, CN · Registration 3007309332

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
3007309332
FEI Number
3007309332
Entity Name
SHANGHAI SHIFT ELECTRICS CO.,LTD.
City/State/Country
SHANGHAI, CN
Establishment Address
No.489 Jinbai Road, SHANGHAI 201506, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
SHANGHAI SHIFT ELECTRICS CO.,LTD. (Owner Number: 10027295)
Owner / Operator Contact Address
No.489 Jinbai Road, SHANGHAI, CN-SH 201506, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MAXPOWER ELECTRIC TOOTHBRUSH, model K1632SW

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JEQ Toothbrush, Powered Dental Class 1 872.6865 2008-10-22
EFW Toothbrush, Manual Dental Class 1 872.6855 2009-10-28

Official Correspondent

GOJA XU

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

SHANGHAI SHIFT ELECTRICS CO.,LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015282468 Koln&Shift Private Limited TripleOne Somerset South East, SG

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007309332. Last updated year: 2026. Please use registration number 3007309332 when referencing this establishment in official correspondence.
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