Data / Medical devices / Hong Kong / Hopstech Industries Ltd
Hopstech Industries Ltd: FDA-registered device maker in Kwun Tong, Kowloon, Hong Kong, Hong Kong, 1 510(k) clearance
Hopstech Industries Ltd is registered with the FDA (registration 3007740394) in Kwun Tong, Kowloon, Hong Kong, Hong Kong. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 26, 2007. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007740394
- Address
- Rm 1411,Blk A, 14/F,Hoi Luen Ind. center 55 Hoi Yuen Road, Kwun Tong, Kowloon, Hong Kong, Hong Kong, 999077
- Owner or operator
- China Inspiration Ltd. (10046636)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 20, 2014
- Registered through
- 2027
- Brand names listed
- Bumpy Ball, PSI bands, Puffer Itch Roller, Scratch Attack Roller, Scratch Star, Talk Tools
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Acupressure | MVV | U | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Monitor, Bed Patient | KMI | 1 | Contract manufacturer | accessdata.fda.gov |
| Operating Room Accessories Table Tray | FWZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 26, 2007 | K070766 | PSI BANDS | MVV | Substantially Equivalent | Psi Health Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Manual
- All makers of Monitor, Bed Patient
- All makers of Device, Acupressure
- All makers of Vibrator, Therapeutic
- All makers of Operating Room Accessories Table Tray
Updated July 26, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.