Manufacturer registered with FDA

Shenzhen Shuye Technology Co.,Ltd

Shenzhen, China. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10088706Manufacturer
Device types listed
1
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
22 registrations outside the US
Establishments
1China

Registered in 2 markets

Where regulators' registries name Shenzhen Shuye Technology Co.,Ltd as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedCanada: 2 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerShenzhen Shuye Technology Co.,Ltd1 device types—Below
CanadaHealth CanadaRegistration holderSHENZHEN SHUYE TECHNOLOGY CO.,LTD.22026–2026Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Shenzhen Shuye Technology Co.,Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
LaifenLaifen Wave Electric Toothbrush LFTB01-P LFTB01-A LFTB01-S LFTB01-TLaifen Wave Pro Electric Toothbrush LFTB02-P LFTB02-A LFTB02-S LFTB02-PTLaifen Wave SE Electric Toothbrush LFTB01 SE
2023

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
ZHUHAI LAIFEN TECHNOLOGY CO.,LIMITEDFDA reg. 3029952413Zhuhai Guangdong, ChinaManufacturer

Other names on FDA records

Zhuhai Laifen Technology Co.,limited

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10088706). 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.