Manteia Technologies Co L T D

FDA Filings

This page includes the latest FDA filings for Manteia Technologies Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3016686005
FEI Number3016686005
NameMarco Mu
Owner & OperatorManteia Technologies Co.,Ltd.
Contact Address1903, B Tower, Zijin Plaza, No.1811 Huan
Xiamen CN-35 Fujian 361000 CN
Official Correspondent
  • Chao Fang
  • 086-0592-6100813-x
US Agent
  • Marco Mu
  • 360 3257028
  • us.agent@mid-link.net
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2219 Rimlang Drive, Suite 301, Bellingham-Barkley Villiage, WA,
Bakerview, WA 98226 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Manteia Technologies Co.,Ltd.
MOZI TPS 2023-11-14
Manteia Technologies Co.,Ltd.
AccuCheck 2023-11-14
Manteia Technologies Co.,Ltd.
AccuContour 2023-04-10
Manteia Technologies Co.,Ltd.
AccuContour 2020-06-30
Marco Mu [Manteia Technologies Co.,Ltd.]
AccuContour2020-03-11

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.