Pepin Mfg Inc

FDA Filings

This page includes the latest FDA filings for Pepin Mfg 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: 2132556
• FEI Number: 1000221051
• Name: PEPIN MFG., INC.
• Owner & Operator: PEPIN MFG., INC.
• Contact Address: 1875 HWY 61 SOUTH --; Lake City MN 55041 US
• Official Correspondent:
  • Melissa - Ryan
  • x-651-3455655-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 1875 HWY 61 SOUTH ; LAKE CITY, MN 55041 US
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
PMN K070807 | GXY PEPIN MFG., INC.	CUTANEOUS ELECTROTHERAPY	2007-08-10
PMN K070807 | GXY PEPIN MFG., INC.	AdvanTrode?	2007-08-10
PMN K070807 PEPIN MFG., INC.	CUTANEOUS ELECTROTHERAPY AND RECORDING ELECTRODES; TENS ELECTRODES	2007-05-23
PMN K060579 PEPIN MFG., INC.	COMFORT/IO IONTOPHORESIS ELECTRODES	2006-04-20
PMN K932849 PEPIN MFG., INC.	PMI TENS ELECTRODE	1994-01-27