Data / Medical devices / China / Digital Dental Depot

Digital Dental Depot: FDA-registered device maker in zhuhai Guangdong, China, 3 510(k) clearances

Name: Digital Dental Depot FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Digital Dental Depot is registered with the FDA (registration 3011170140) in zhuhai Guangdong, China. It lists 17 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: 3011170140
Address: 10 pingbei 1st Rd, Nanping science and technology park Zhuhai, zhuhai Guangdong, China, 519000
Owner or operator: Digital Dental Depot (10047277)
Roles: Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
First device listed: July 31, 2014
Registered through: 2026
Brand names listed: Accessories, implant, dental Endosseous, Alloy, Gold Based Nobel Metal, Alloy, Metal, Base, Dentures, Full, Dentures, partial, Device, jaw repositioning, Prosthesis, orthodontic, Restoration, Base Metal and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Implant, Dental, Endosseous	NDP	1	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Alloy, Gold-Based Noble Metal	EJT	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Alloy, Metal, Base	EJH	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Alloy, Other Noble Metal	EJS	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Dentures, Full	NSL	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Dentures, Partial	NSK	N	Contract manufacturer, Manufacturer, Repackager or relabeler	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, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Prosthesis, Orthodontic	NSR	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Restoration, Base Metal	NSQ	N	Contract manufacturer	accessdata.fda.gov
Restoration, Noble Metal	NSJ	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Restoration, Porcelain	NSP	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Restoration, Porcelain-Fused-To-Metal	NSO	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Restoration, Resin, Crown And Bridge	NSN	N	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations	NOF	2	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Wax, Dental, Intraoral	EGD	1	Contract manufacturer, Manufacturer, Repackager or relabeler	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

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.