Manufacturer registered with FDA

Nanning Sixtant Biotechnology Co., Ltd

Nanning, China. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10085641Foreign exporterManufacturer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
32 registrations outside the US
Establishments
1China

Registered in 3 markets

Where regulators' registries name Nanning Sixtant Biotechnology Co., Ltd as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedAustralia: 1 registrationsUnited Kingdom: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerNanning Sixtant Biotechnology Co., Ltd2 device types—Below
AustraliaTGAManufacturerNanning Sixtant Biotechnology Co Ltd12025–2025Pure Global AI
United KingdomMHRAManufacturerNanning Sixtant Biotechnology Co., Ltd1—Pure 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 Nanning Sixtant Biotechnology Co., Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Manual ToothbrushEFW · Class 1ToothbrushesMaker
Water flosser
2023
Powered Tongue ScraperQIA · Class 1—Maker
Tooth paste
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
NANNING SIXTANT BIOTECHNOLOGY CO., LTDFDA reg. 3023855650Nanning Guangxi, ChinaForeign exporter, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10085641). 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.