Data / Medical devices / Hong Kong / Digital Dental Depot Limited
Digital Dental Depot Limited: FDA-registered device maker in Hong Kong, Hong Kong, 3 510(k) clearances
Digital Dental Depot Limited is registered with the FDA (registration 3012341864) in Hong Kong, Hong Kong. It lists 16 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 11, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012341864
- Address
- 702, Cheong Hing Building, 72 Nathan Road Tst, Hong Kong, Hong Kong, 999077
- Owner or operator
- Digital Dental Depot Limited (10055428)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- July 24, 2017
- Registered through
- 2026
- Brand names listed
- ALLOY, METAL, BASE, ALLOY, OTHER NOBLE METAL, Advanced Anti-Snoring Device 4 Clear/Blue, Alloy, gold-based noble metal, Anti-Snoring Device, DRILL, DENTAL, INTRAORAL, DZA / DRILL, DENTAL, INTRAORAL, Dentures, partial and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Alloy, Gold-Based Noble Metal | EJT | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Alloy, Metal, Base | EJH | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Alloy, Other Noble Metal | EJS | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Dentures, Partial | NSK | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Anti-Snoring | LRK | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Device, Jaw Repositioning | LQZ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Prosthesis, Orthodontic | NSR | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Base Metal | NSQ | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Noble Metal | NSJ | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain | NSP | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain-Fused-To-Metal | NSO | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Resin, Crown And Bridge | NSN | N | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations | NOF | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wax, Dental, Intraoral | EGD | 1 | Contract manufacturer, Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| June 11, 2026 | K261251 | Snorbliss® Anti-Snoring Device | LRK | Substantially Equivalent | Endeavor Commerce, LLC | accessdata.fda.gov |
| May 14, 2026 | K261134 | Dormiva Anti-Snoring Mouth Guard | LRK | Substantially Equivalent | Koncept Innovators, Inc. | accessdata.fda.gov |
| May 8, 2025 | K250482 | Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue | LRK | Substantially Equivalent | Fissiontech, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Restoration, Porcelain
- All makers of Drill, Dental, Intraoral
- All makers of Dentures, Partial
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Restoration, Noble Metal
- All makers of Device, Jaw Repositioning
Updated June 11, 2026. 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.