Manufacturer registered with FDA

Shen FU Arts Lab

Shen Zhen, China. Lists 6 dental device types with FDA across 1 registered establishment.

FDA owner/operator9063832Manufacturer

Device types listed: 6
Brands and models: 0
510(k) clearances: 0as applicant
Markets registered in: 1United States
Establishments: 1China

Devices listed with FDA

What Shen FU Arts Lab currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Rebasing Repairing Relining Denture ResinEBI · Class 2	Denture resins & teeth	Maker	—	2016
Intraoral Dental WaxEGD · Class 1	—	Maker	—	2010
Base Metal AlloyEJH · Class 2	Dental alloys	Maker	—	2007
Alloy Other Noble MetalEJS · Class 2	Dental alloys	Maker	—	2007
Gold-Based Noble Metal AlloyEJT · Class 2	Dental alloys	Maker	—	2004
Computer Assisted Design and Manufacturing (Cad/Cam) of Dental Restorations Optical Impression SystemNOF · Class 2	Intraoral scanners	Maker	—	2010

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Also lists devices cleared under other names

Shen FU Arts Lab lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Dentsply Intl., Inc. (1).

Decided	510(k)	Device	Applicant	Device type
12 Mar 1980	K800400	MAXUM DENTURE RESIN	Dentsply Intl., Inc.	EBI Rebasing Repairing Relining Denture Resin

Registered establishments

Establishment	Location	What it does
SHEN FU ARTS LABFDA reg. 3004578725	Shen Zhen Guangdong, China	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9063832). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.