Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027518284

FEI Number

3027518284

Entity Name

FORETHOUGHT(SHANGHAI)MEDICAL TECHNOLOGY CO., LTD.

City/State/Country

Shanghai, CN

Establishment Address

Room B9, 8th Floor, Kehai Building, No.800 Naxian Road, Pudong New Area, Shanghai, China, Shanghai 201203, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Forethought(Shanghai)Medical Technology Co., Ltd. (Owner Number: 10087972)

Owner / Operator Contact Address

Room B9, 8th Floor, Kehai Building, No.800 Naxian Road, Pudong New Area, Shanghai, China, Shanghai, CN-SH 201203, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Forethought ScoliMatrix 3D Detection System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2023-05-08

Official Correspondent

Feifei Zhu

US Agent Details

Jemes Wang Business: LLINS TECHNOLOGY INC Email: fda-rep@llins-tech.com Phone: (720) 2171916

Related Public Records

Same Entity

Forethought(Shanghai)Medical 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 3027518284. Last updated year: 2026. Please use registration number 3027518284 when referencing this establishment in official correspondence.