Jerry Lee

FDA Filings

This page includes the latest FDA filings for Jerry Lee. 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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Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020061529023Yantian,China (Mainland) -> Oakland, CaliforniaLASERSIGHT1 PCS
2020050157619Yantian,China (Mainland) -> Oakland, CaliforniaIRONS KKS52151411 PCS
2020050172213Yantian,China (Mainland) -> Oakland, CaliforniaLADIES COAT1 PCS
2020042571404Yantian,China (Mainland) -> Oakland, CaliforniaSCREEN PROTECTOR1 PCS
2020042469496Yantian,China (Mainland) -> Oakland, CaliforniaSCREEN PROTECTOR1 PCS
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