Manufacturer registered with FDA

Ningbo kingworth global imp & exp co.,ltd

Ningbo, China. Lists 5 dental device types with FDA across 0 registered establishments.

FDA owner/operator10096559Foreign exporterManufacturer
Device types listed
5
Brands and models
7
510(k) clearances
0as applicant
Markets registered in
21 registrations outside the US
Establishments
0—

Registered in 2 markets

Where regulators' registries name Ningbo kingworth global imp & exp co.,ltd as the manufacturer or the registration holder of a device.

All markets
United States: 5 device types listedEuropean Union: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerNingbo kingworth global imp & exp co.,ltd5 device types—Below
European UnionEUDAMEDManufacturerNingBo KingWorth Global Imp. & Exp. 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 Ningbo kingworth global imp & exp co.,ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Oral Irrigation UnitEFS · Class 1Oral irrigatorsMaker
Powered Dental FlosserWater Flosser
2026
Manual ToothbrushEFW · Class 1ToothbrushesMaker
Manual Toothbrush
2026
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
Powered ToothbrushSonic Electric Toothbrush
2026
Dental FlossJES · Class 1Floss & interdental cleanersMaker
Dental Floss
2026
Massaging PickJET · Class 1Floss & interdental cleanersMaker
Dental Pick
2026

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

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10096559). 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.