Crosstech Diamond Tools Co L T D

FDA Filings

This page includes the latest FDA filings for Crosstech Diamond Tools 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 Number3004362293
FEI Number3004362293
NameCROSSTECH DIAMOND TOOLS CO., LTD.
Owner & OperatorCROSSTECH DIAMOND TOOLS CO., LTD.
Contact Address109/87 MOO 2 TEPARAK ROAD SAMUTPRAKRAN
BANGSAOTHONG TH-NOTA 10540 TH
US Agent
  • Linda Laine
  • 408 4552150
  • 800 3490728
  • linda0laine@gmail.com
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address109/87 MOO 2 TEPARAK ROAD SAMUTPRAKRAN
Samutprakran Samut Prakan, 10540 TH
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
CROSSTECH DIAMOND TOOLS CO., LTD.
CRYSTAL DIAMOND INSTRUMENTS2003-12-03

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