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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

DeviceProduct codeClassRoleSource
Accessories, Implant, Dental, EndosseousNDP1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Alloy, Gold-Based Noble MetalEJT2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Alloy, Metal, BaseEJH2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Alloy, Other Noble MetalEJS2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Dentures, PartialNSKNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Device, Anti-SnoringLRK2Exporter to the US, Manufactureraccessdata.fda.gov
Device, Jaw RepositioningLQZ2Exporter to the US, Manufactureraccessdata.fda.gov
Drill, Dental, IntraoralDZA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Prosthesis, OrthodonticNSRNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Restoration, Base MetalNSQNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Restoration, Noble MetalNSJNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Restoration, PorcelainNSPNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Restoration, Porcelain-Fused-To-MetalNSONContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Restoration, Resin, Crown And BridgeNSNNContract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental RestorationsNOF2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Wax, Dental, IntraoralEGD1Contract manufacturer, Exporter to the US, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 11, 2026K261251Snorbliss® Anti-Snoring DeviceLRKSubstantially EquivalentEndeavor Commerce, LLCaccessdata.fda.gov
May 14, 2026K261134Dormiva Anti-Snoring Mouth GuardLRKSubstantially EquivalentKoncept Innovators, Inc.accessdata.fda.gov
May 8, 2025K250482Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 BlueLRKSubstantially EquivalentFissiontech, LLCaccessdata.fda.gov

Compare with other makers

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.