Keith Huang

FDA Filings

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

FDA Registration(s)

• Registration Number: 3013433000
• FEI Number: 3013433000
• Name: Keith Huang
• Owner & Operator: PreXion Corporation
• Contact Address: 1-14-1, Kandasuda-cho ; Chiyoda-ku JP-13 Tokyo 101-0041 JP
• Official Correspondent:
  • Kenji Tanaka
  • 81-3-52977551-x
• US Agent:
  • Keith Huang
  • 650 2120300
  • khuang@PreXion.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2077 Gateway Place, Suite 120 ; San Jose, CA 95110 US
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

• Registration Number: 3009191416
• FEI Number: 3009191416
• Name: Keith Huang
• Owner & Operator: PreXion Corporation
• Contact Address: 1-14-1, Kandasuda-cho ; Chiyoda-ku JP-13 Tokyo 101-0041 JP
• Official Correspondent:
  • Kenji Tanaka
  • 81-3-52977551-x
• US Agent:
  • Keith Huang
  • PreXion,Inc.
  • 650 2120300
  • khuang@prexion.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2077 Gateway Place, Suite 120 ; San Jose, CA 95110 US
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
PMN K190320 | OAS Keith Huang [PreXion Corporation]	PreXion3D Explorer	2019-04-16
PMN K161881 | OAS Keith Huang [PreXion Corporation]	PreXion3D Excelsior	2016-10-12

Similar & Related FDA Registered Companies

• PreXion,Inc.