Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012191011

FEI Number

3012191011

Entity Name

GYENNO TECHNOLOGIES CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

801-804 & 904, Building B2, Phase II, Creative City, Xian Dong Road, Xili Street, Nanshan District, Shenzhen,, Shenzhen Guangdong 518055, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GYENNO Technologies CO., LTD. (Owner Number: 10049980)

Owner / Operator Contact Address

801-804 & 904, Building B2, Phase II, Creative City, Xian Dong Road, Xili Street, Nanshan District, Shenzhen,, Shenzhen, CN-GD 518055, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hand Tremor Data Collector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILC	Utensil, Eating	Physical Medicine	Class 1	890.5050	2015-09-24

Official Correspondent

Liu qiaojuan

US Agent Details

Cecilia Zhou Email: Cecilia.zhou@gmail.com Phone: (646) 3383683

Related Public Records

Same Entity

GYENNO Technologies 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 3012191011. Last updated year: 2026. Please use registration number 3012191011 when referencing this establishment in official correspondence.