Manufacturer registered with FDA

Evereast Medical Products Group Co., Ltd

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

FDA owner/operator10063920Contract manufacturerForeign exporterManufacturer
Device types listed
1
Brands and models
6
510(k) clearances
0as applicant
Markets registered in
4107 registrations outside the US
Establishments
1China

Registered in 4 markets

Where regulators' registries name Evereast Medical Products Group Co., Ltd as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedBrazil: 102 registrationsSaudi Arabia: 4 registrationsColombia: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerEvereast Medical Products Group Co., Ltd1 device types—Below
BrazilANVISAManufacturerEVEREAST MEDICAL PRODUCTS GROUP CO. LTD.1022019–2026Pure Global AI
Saudi ArabiaSFDAManufacturerEvereast Medical Products Group Co.,LTD4—Pure Global AI
ColombiaINVIMAManufacturerEVEREAST MEDICAL PRODUCTS GROUP CO., LTD.1—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 Evereast Medical Products Group Co., Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Paper Saliva AbsorberKHR · Class 1—Maker
Baby bibsdental aprondental bibsDisposable bibspaper dental bibsProtection Sheet
2024

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
EVEREAST MEDICAL PRODUCTS GROUP CO., LTDFDA reg. 3016195240Changyuan City Henan, ChinaContract manufacturer, Foreign exporter, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10063920). 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.