Wei Zhang

FDA Filings

This page includes the latest FDA filings for Wei Zhang. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3015537335
FEI Number3015537335
NameWei Zhang
Owner & OperatorKennametal Stellite (Shanghai) Co.,Ltd
Contact AddressNo.1799,JiaLuo Road,JiaDing District,Sha
Shanghai CN-31 Shanghai 201800 CN
Official Correspondent
  • Yonghua Hu
  • 86-21-39523831-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3302 171st Pl Se
Bothell, WA 98012 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Wei Zhang [Kennametal Stellite (Shanghai) Co.,Ltd]
Nickel-Chromium Ceramic Dental Alloy (Stellite N9)2019-07-01
Wei Zhang [Kennametal Stellite (Shanghai) Co.,Ltd]
Cobalt-Chromium Partial Dental Alloy (Stellite C3)2019-07-01

Similar & Related FDA Registered Companies

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020050177381Yantian,China (Mainland) -> Oakland, CaliforniaGLASSES1 PCS
2020050177591Yantian,China (Mainland) -> Oakland, CaliforniaPHONE ACCESSORIES1 PCS
2020050177767Yantian,China (Mainland) -> Oakland, CaliforniaACUPUNCTURE NEEDLE1 PCS
2020050177875Yantian,China (Mainland) -> Oakland, CaliforniaESSENTIAL OIL1 PCS
2020042949994Yantian,China (Mainland) -> Oakland, CaliforniaCASES1 PCS
2020042789883Yantian,China (Mainland) -> Oakland, CaliforniaSPORT FACE MASK1 PCS
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