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 Number: 3016686005
• FEI Number: 3016686005
• Name: Marco Mu
• Owner & Operator: Manteia Technologies Co.,Ltd.
• Contact Address: 1903, 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 Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2219 Rimlang Drive, Suite 301, Bellingham-Barkley Villiage, WA, ; Bakerview, WA 98226 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 06973127400029 Manteia Technologies Co.,Ltd.	AccuContour	2025-06-24
GUDID 06973127400067 Manteia Technologies Co.,Ltd.	MOZI TPS	2023-11-14
GUDID 06973127400043 Manteia Technologies Co.,Ltd.	AccuCheck	2023-11-14
GUDID 06973127400050 Manteia Technologies Co.,Ltd.	AccuContour	2023-04-10
GUDID 16973127400019 Manteia Technologies Co.,Ltd.	AccuContour	2020-06-30
PMN K191928 | QKB Marco Mu [Manteia Technologies Co.,Ltd.]	AccuContour	2020-03-11