Manufacturer registered with FDA

Weihai Xingtai Packaging Products Co., Ltd.

WeiHai, China. Lists 5 dental device types with FDA across 1 registered establishment.

FDA owner/operator10074054Manufacturer
Device types listed
5
Brands and models
5
510(k) clearances
0as applicant
Markets registered in
33 registrations outside the US
Establishments
1China

Registered in 3 markets

Where regulators' registries name Weihai Xingtai Packaging Products Co., Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 5 device types listedEuropean Union: 2 registrationsIsrael: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerWeihai Xingtai Packaging Products Co., Ltd.5 device types—Below
European UnionEUDAMEDManufacturerWEIHAI XINGTAI PACKAGING PRODUCTS CO.,LTD.2—Pure Global AI
IsraelAMARManufacturerWeihai Xingtai Packaging Products 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 Weihai Xingtai Packaging Products Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Saliva Ejector MouthpieceDYN · Class 1—Maker
Saliva ejector
2024
Roll CottonEFN · Class 1—Maker
Dental cotton roll
2024
X-Ray Film HolderEGZ · Class 1—Maker
Barrier Film
2024
Prophylaxis CupEHK · Class 1Polishing & prophylaxisMaker
Prophy angle
2024
Paper Saliva AbsorberKHR · Class 1—Maker
Denal Apron;Dental bibs
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
WEIHAI XINGTAI PACKAGING PRODUCTS CO., LTD.FDA reg. 3017220525WeiHai Shandong, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10074054). 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.