Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007092044

FEI Number

3007092044

Entity Name

TYECE LIMITED

City/State/Country

Kowloon, HK

Establishment Address

Unit 803, Block A, Po Lung Centre, 11 Wang Chiu Rd, Kowloon Bay, Kowloon HKG, HK

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Tyece Limited (Owner Number: 10031685)

Owner / Operator Contact Address

Unit 803, Block A, Po Lung Centre, 11 Wang Chiu Rd, Kowloon Bay, Kowloon, HK-NOTA HKG, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172241

PMA Number

N/A

All Registered Proprietary Names

TENS/EMS TENS/EMS ELC TENS/EMS TENS/EMS TENS/EMS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2019-03-02
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2014-02-05
LJL	Detectors And Removers, Lice, (Including Combs)	General Hospital	Class 1	880.5960	2015-05-29
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2020-08-13
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2016-11-25
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2020-12-15

Official Correspondent

Parshid Falahati

US Agent Details

Peter Isaac Email: peter.isaac@pi-international.com Phone: (630) 5701449

Related Public Records

Same Entity

Tyece Limited

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
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007092044. Last updated year: 2026. Please use registration number 3007092044 when referencing this establishment in official correspondence.