Poonglim Pharmatech Inc

FDA Filings

This page includes the latest FDA filings for Poonglim Pharmatech Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3014149127
• FEI Number: 3014149127
• Name: Peter Chung
• Owner & Operator: Poonglim Pharmatech Inc.
• Contact Address: 21, Jayumuyeok 1-gil ; Gunsan-si KR-45 Jeonrabugdo 54001 KR
• Official Correspondent:
  • Hee Min Cho
  • 82-63-4518141-x
• US Agent:
  • Peter Chung
  • PlusGlobal
  • 412 5128802
  • peterchung210@gmail.com
• Importing Logistics Registration:
  • Importer: Plus Global
  • Address: 300 Atwood ; Pittsburgh, PA 15213 UNITED STATES
  • Phone: 1 412 5128802
  • Importer Type: AGENT
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 300 Atwood St. ; Pittsburgh, PA 15213 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K210444 Poonglim Pharmatech Inc.	EZ-Injec LDV Sterile Safety Needle	2021-02-16
PMN K192222 POONGLIM Pharmatech Inc.	EZ-Inject Single Use Needle	2020-05-12
PMN K172483 | FMI Peter Chung [Poonglim Pharmatech Inc.]	Kopac Sterile Needle	2020-03-26
PMN K172483 Poonglim Pharmatech Inc.	Kopac Sterile Needle	2018-06-21