HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO.,

FDA Device Registration & Listing · XIAMEN Fujian, CN · Registration 3005607635

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
3005607635
FEI Number
3005607635
Entity Name
HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO.,
City/State/Country
XIAMEN Fujian, CN
Establishment Address
No. 5, Haijing Dongsan Road, Bonded Port Area Xiamen Area of Polit Free Trade Zone, XINGGANG RD.,HAICANG DISTRICT, XIAMEN Fujian 361026, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO., (Owner Number: 9083459)
Owner / Operator Contact Address
EXPORT PROCESSING ZONE, NO.5, XINGGANG RD.,HAICANG DISTRICT, XIAMEN, CN-NOTA 361026, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

COLGATE POWERED TOOTHBRUSH quip Rechargeable Water Flosser COLGATE MANUAL TOOTHBRUSH COLGATE OPTIC WHITE PROFESSIONAL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JEQ Toothbrush, Powered Dental Class 1 872.6865 2006-02-27
EFS Unit, Oral Irrigation Dental Class 1 872.6510 2022-05-24
EFW Toothbrush, Manual Dental Class 1 872.6855 2018-02-28
JES Floss, Dental Dental Class 1 872.6390 2020-09-03
EEG Heat Source For Bleaching Teeth Dental Class 1 872.6475 2018-02-28
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2021-01-27

Official Correspondent

No official correspondent registered.

US Agent Details

YUETING ZHU Business: SOUTH BAY INNOVATION LLC Email: southbayinnovation@southbayinnovation.com Phone: (424) 3769142

Related Public Records

Same Entity

HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO.,
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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005607635. Last updated year: 2026. Please use registration number 3005607635 when referencing this establishment in official correspondence.
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