XIAMEN JIEBOYA TECHNOLOGY CO.LTD

FDA Device Registration & Listing · Xiamen Fujian, CN · Registration 3015456958

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
3015456958
FEI Number
3015456958
Entity Name
XIAMEN JIEBOYA TECHNOLOGY CO.LTD
City/State/Country
Xiamen Fujian, CN
Establishment Address
R.301, No.39-1 Qingfeng Road,, Guankou Town, Jimei District, Xiamen Fujian 361000, CN
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
XiaMen Jieboya Technology Co.Ltd (Owner Number: 10060279)
Owner / Operator Contact Address
R.301, No.39-1 Qingfeng Road,, Guankou Town, Jimei District, Xiamen, CN-FJ 361000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

T011XX,T012XX,T021XX,TX022XX,TX031XX,T032XX,T041XX, T042XX,T051XX,T052XX,RTG02, RTG02RP, RTG02XX W061XX,W062XX,W071XX,W072XX,W091XX,W092,W092XX,W094,W094XX, GO-100, WJ14MN W011XX(JR00302),W012XX(JR00102),W013XX(JR00002),W021XX(JY00300),W022XX(JY00100),W023XX(JY0000),W041XX,W042XX,W054XX,WJ15 A01XX RTGX01,RTGX01XX RTGXRP01,RTGXRP01XX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMD Toothbrush, Ionic, Battery-Powered Dental Class 1 872.6865 2019-04-19
EFS Unit, Oral Irrigation Dental Class 1 872.6510 2019-07-24
JET Pick, Massaging Dental Class 1 872.6650 2019-04-19
JEQ Toothbrush, Powered Dental Class 1 872.6865 2021-12-30

Official Correspondent

Suiqing Chen

US Agent Details

Jessie Peng Business: Mars Business Consulting, LLC Email: jessie@registeragentllc.com Phone: (858) 9050218

Related Public Records

Same Entity

XiaMen Jieboya 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
K821629 Moyco Industries, Inc. FIXIDENT 1982-06-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015456958. Last updated year: 2026. Please use registration number 3015456958 when referencing this establishment in official correspondence.
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