Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010975837

FEI Number

3010975837

Entity Name

TOPARC TECHNOLOGY (SHENZHEN) CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Nbr. 101; 1-4 Floors of Workshop; Nbr 23-1 Longteng Road, Baoan Community Yuanshan Street; Shenzhen, GUANGDONG, Shenzhen Guangdong 518115, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

TOPARC TECHNOLOGY (SHENZHEN) CO.,LTD (Owner Number: 10051042)

Owner / Operator Contact Address

Nbr.101; 1-4 Floors Of Workshop; Nbr. 23-1 Longteng Road,, Baoan Community Yuanshan Street, Longgang, Shenzhen, CN-GD 518115, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Vibrator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IRO	Vibrator, Therapeutic	Physical Medicine	Class 1	890.5975	2016-01-28

Official Correspondent

Manesh Daryanani

US Agent Details

KRISTIAN BROMS Business: PIPEDREAM PRODUCTS LLC Email: KRISTIAN@DIAMONDPROD.COM Phone: (818) 2598841

Related Public Records

Same Entity

TOPARC TECHNOLOGY (SHENZHEN) CO.,LTD

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
K821133	Durham Electric Co.	ELECTRICAL VIBRATING DEVICE	1982-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010975837. Last updated year: 2026. Please use registration number 3010975837 when referencing this establishment in official correspondence.