Kaiwood Technology Co L T D

FDA Filings

This page includes the latest FDA filings for Kaiwood Technology 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 Number3006397937
FEI Number3006397937
NameJerry Lee
Owner & OperatorKAIWOOD TECHNOLOGY CO., LTD.
Contact Address5F, N.12, LANE 31, SEC. 1 HUONGDUNG RD
HSIN-SHI, TAINAN COUNTY TW-NOTA 74146 TW
Official Correspondent
  • PI-YAO - TING
  • 886-6-6006000-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2782 Loker Ave West
Carlsbad, CA 92010 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Jerry Lee [KAIWOOD TECHNOLOGY CO., LTD.]
Portable Ovulation Device2018-08-05
Jerry Lee [KAIWOOD TECHNOLOGY CO., LTD.]
LUMINOMETER2007-01-17
Jerry Lee [KAIWOOD TECHNOLOGY CO., LTD.]
RAPID TEST READER2007-01-17
Jerry Lee [KAIWOOD TECHNOLOGY CO., LTD.]
CHROMOGENIC STRIP DECTECTION SYSTEM2007-01-17

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