Data / Medical devices / Hong Kong / BND Limited
BND Limited: FDA-registered device maker in Hong Kong, Hong Kong, 1 510(k) clearance
BND Limited is registered with the FDA (registration 3007186430) in Hong Kong, Hong Kong. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007186430
- Address
- Flat B, 6/F, Tong Yuen Factory Building, 505 Castle Peak Road, Lai Chi Kok, Hong Kong, Hong Kong, -
- Owner or operator
- BND Limited (10054020)
- Roles
- Exporter to the US
- First device listed
- February 1, 2017
- Registered through
- 2026
- Brand names listed
- CASE, CONTACT LENS, FLOSS, DENTAL, Hot or cold; reusable pack, Intraoral Dental Wax, Sunglasses, TOOTHBRUSH
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Case, Contact Lens | LRX | 2 | Exporter to the US | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Exporter to the US | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Exporter to the US | accessdata.fda.gov |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | Exporter to the US | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Exporter to the US | accessdata.fda.gov |
| Wax, Dental, Intraoral | EGD | 1 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| May 1, 2007 | K071081 | CONTACT LENS CASE | LRX | Substantially Equivalent | Ningbo Kaida Rubber and Plastic Technology Co., LT | accessdata.fda.gov |
Compare with other makers
- All makers of Sunglasses (Non-Prescription Including Photosensitive)
- All makers of Case, Contact Lens
- All makers of Floss, Dental
- All makers of Toothbrush, Manual
- All makers of Wax, Dental, Intraoral
- All makers of Pack, Hot Or Cold, Reusable
Updated May 1, 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.