HOPSTECH INDUSTRIES LTD

FDA Device Registration & Listing · Kwun Tong, Kowloon, Hong Kong, HK · Registration 3007740394

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007740394
FEI Number
3007740394
Entity Name
HOPSTECH INDUSTRIES LTD
City/State/Country
Kwun Tong, Kowloon, Hong Kong, HK
Establishment Address
Rm 1411,Blk A, 14/F,Hoi Luen Ind. center, 55 Hoi Yuen Road, Kwun Tong, Kowloon, Hong Kong 999077, HK
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
China Inspiration Ltd. (Owner Number: 10046636)
Owner / Operator Contact Address
Jiekou Industrial District, Changan, Dongguan, Guangdong, China, dongguan, CN-GD 523850, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Talk Tools PSI bands Puffer Itch Roller Bumpy Ball Scratch Star Scratch Attack Roller

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2016-02-16
KMI Monitor, Bed Patient General Hospital Class 1 880.2400 2014-04-20
MVV Device, Acupressure Unknown Class U N/A 2022-09-06
FWZ Operating Room Accessories Table Tray General, Plastic Surgery Class 1 878.4950 2014-06-16
LYG Massager, Therapeutic, Manual Physical Medicine Class 1 890.5660 2025-12-23

Official Correspondent

Rita Chung

US Agent Details

Jerry Doane Business: Pragmatic Compliance dba FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

China Inspiration 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 3007740394. Last updated year: 2026. Please use registration number 3007740394 when referencing this establishment in official correspondence.
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