Pinnacle Co L T D

FDA Filings

This page includes the latest FDA filings for Pinnacle 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 Number3006946173
FEI Number3006946173
NameKen Li
Owner & OperatorPinnacle Co., Ltd
Contact AddressLot 2, No. 21 Qingtian Road Qilu Chemical Industrial Park
Linzi, Zibo CN-37 Shandong 255414 CN
Official Correspondent
  • David Ding
  • 86-533-7489957-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address35 Constitution Drive, Suite 1D
Bedford, NH 03110 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
PINNACLE CO., LTD.
VINYL EXAMINATION GLOVE, POWDERED2008-02-21
PINNACLE CO., LTD.
VINYL EXAMINATION GLOVE POWDER FREE2008-02-15
Ken Li [Pinnacle Co., Ltd]
omnishield2008-02-15
Ken Li [Pinnacle Co., Ltd]
Omnishied2008-02-15
Ken Li [Pinnacle Co., Ltd]
omnishield2008-02-15
PINNACLE CO., LTD.
SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE)2008-02-08

Similar & Related FDA Registered Companies

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.