Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038138206

FEI Number

3038138206

Entity Name

HIPPOSCREEN NEUROTECH CORP.

City/State/Country

Neihu Dist. Taipei, TW

Establishment Address

2F., No.578, Ruiguang Rd., Neihu Dist. Taipei 114, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

HippoScreen Neurotech Corp. (Owner Number: 10093103)

Owner / Operator Contact Address

2F., No.578, Ruiguang Rd., Neihu Dist., TW-TPE 114, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K201747

PMA Number

N/A

All Registered Proprietary Names

8-CH Electroencephalography Amplifier

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWL	Amplifier, Physiological Signal	Neurology	Class 2	882.1835	2025-03-31
OMC	Reduced- Montage Standard Electroencephalograph	Neurology	Class 2	882.1400	2025-03-31

Official Correspondent

Amber Dong

US Agent Details

Chun-Kai Yang Email: ra733015@gmail.com Phone: (580) 8780111

Related Public Records

Same Entity

HippoScreen Neurotech Corp.

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 3038138206. Last updated year: 2026. Please use registration number 3038138206 when referencing this establishment in official correspondence.