Suzhou Jenitek Precision Device Co L T D

FDA Filings

This page includes the latest FDA filings for Suzhou Jenitek Precision Device 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 Number: 3013921506
• FEI Number: 3013921506
• Name: Simcal
• Owner & Operator: SUZHOU JENITEK PRECISION DEVICE CO.,LTD.
• Contact Address: EMeiShan Road,SND ; Suzhou CN-32 Jiangsu 215153 CN
• Official Correspondent:
  • Jinbo Wang
  • 086-512-6680600-1
• US Agent:
  • Simcal
  • UCL-REG SERVICE INC.
  • 347 7030850
  • gbstandard@163.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 3907 PRINCE STREET SUITE 6F ; Flushing, NY 11354 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 06973102450018 Suzhou Jenitek Precision Device Co., Ltd.	JENITEK	2020-07-14