Manufacturer registered with FDA

Jiangsu Province Yangzhou Shuguang Toothbrush Manu

JANGZHOU, JIANGSU PROVINCE, China. Lists 12 dental device types with FDA across 1 registered establishment.

FDA owner/operator9066595Manufacturer
Device types listed
12
Brands and models
15
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1China

Devices listed with FDA

What Jiangsu Province Yangzhou Shuguang Toothbrush Manu currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsMaker
Aligner Tray SeaterChewies
2020
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
Plastic Mouth Mirror
2011
Orthodontic Band PusherECS · Class 1Dental hand instrumentsMaker
Chewies
2020
Manual ToothbrushEFW · Class 1ToothbrushesMaker
Plastic Toothbrush
2004
Intraoral Dental WaxEGD · Class 1—Maker
Dental Wax
2023
Prophylaxis CupEHK · Class 1Polishing & prophylaxisMaker
Prophy Brush
2020
Oral Cavity EvacuatorEHZ · Class 1Suction & evacuation unitsMaker
Vent O Vac Evacuator Tip
2020
All Types RetractorEIG · Class 1Dental hand instrumentsMaker
LIP PROTECTORRETRATORS
2024
Orthodontic Metal BracketEJF · Class 1Orthodontic bracketsMaker
BRACKETELASTIC PLACER
2024
Dental FlossJES · Class 1Floss & interdental cleanersMaker
Floss
2020
Tongue ScraperLCN · Class 1—Maker
TONGUE SCRAPER
2019
Battery-Powered Ionic ToothbrushMMD · Class 1ToothbrushesMaker
Toothbrush, Battery Powered
2020

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

Registered establishments

EstablishmentLocationWhat it does
JIANGSU PROVINCE YANGZHOU SHUGUANG TOOTHBRUSH MANUFACTORYFDA reg. 3004753334YANG ZHOU Jiangsu, ChinaManufacturer

Other names on FDA records

Jiangsu Province Yangzhou Shuguang Toothbrush Manufactory

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9066595). 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.