Data / Medical devices / Hong Kong / Hongkong Loyal Beauty Technology Limited
Hongkong Loyal Beauty Technology Limited: FDA-registered device maker in Hong Kong, Hong Kong, 1 510(k) clearance
Hongkong Loyal Beauty Technology Limited is registered with the FDA (registration 3015169722) in Hong Kong, Hong Kong. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 12, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015169722
- Address
- ROOMS 1322,13/F Hollywood Plaza,610 Nathan Road, Mongkok, Kowloon, Hong Kong, Hong Kong, 999077
- Owner or operator
- Hongkong Loyal Beauty Technology Limited (10057855)
- Roles
- Exporter to the US
- First device listed
- June 10, 2018
- Registered through
- 2026
- Brand names listed
- CROWN, PREFORMED, Denture, Full, Dentures, partial, Device, Anti-Snoring, Material, Impression Tray, Resin Model, POSITIONER, TOOTH, PREFORMED, Prosthesis, orthodontic, Restoration, base metal and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Crown, Preformed | ELZ | 1 | Exporter to the US | accessdata.fda.gov |
| Dentures, Full | NSL | N | Exporter to the US | accessdata.fda.gov |
| Dentures, Partial | NSK | N | Exporter to the US | accessdata.fda.gov |
| Device, Anti-Snoring | LRK | 2 | Exporter to the US | accessdata.fda.gov |
| Material, Impression Tray, Resin | EBH | 1 | Exporter to the US | accessdata.fda.gov |
| Positioner, Tooth, Preformed | KMY | 1 | Exporter to the US | accessdata.fda.gov |
| Prosthesis, Orthodontic | NSR | N | Exporter to the US | accessdata.fda.gov |
| Restoration, Base Metal | NSQ | N | Exporter to the US | accessdata.fda.gov |
| Restoration, Porcelain-Fused-To-Metal | NSO | N | Exporter to the US | accessdata.fda.gov |
| Restoration, Resin, Crown And Bridge | NSN | N | 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 |
|---|---|---|---|---|---|---|
| July 12, 2006 | K061732 | TAP-T | LRK | Substantially Equivalent | Airway Management, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Material, Impression Tray, Resin
- All makers of Restoration, Porcelain-Fused-To-Metal
- All makers of Positioner, Tooth, Preformed
- All makers of Device, Anti-Snoring
- All makers of Crown, Preformed
- All makers of Dentures, Full
Updated July 12, 2006. 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.