Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3045076539

FEI Number

3045076539

Entity Name

SHENZHEN XINJIANLI TECHNOLOGY CO., LTD.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

3rd Floor, Area B, Honghengjing Fuding Science Park, No.7 Dongsheng Road, Dalingshan Town, Dongguan Guangdong 523000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Shenzhen Xinjianli Technology Co., Ltd. (Owner Number: 10095787)

Owner / Operator Contact Address

3rd Floor, Area B, Honghengjing Fuding Science Park, No.7 Dongsheng Road, Dalingshan Town, Dongguan, CN-GD 523000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Mouth guard, REVIV ONE, REVIV TWO, REVIV THREE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BRW	Protector, Dental	Anesthesiology	Class 1	868.5820	2026-04-28

Official Correspondent

Sharon Wong

US Agent Details

Emilie Davis Email: safjiofewiwds@wilson.ntesmail.com Phone: (805) 5797288

Related Public Records

Same Entity

Shenzhen Xinjianli Technology Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3045076539. Last updated year: 2026. Please use registration number 3045076539 when referencing this establishment in official correspondence.