Pierre Fabre Medical Devices

FDA Filings

This page includes the latest FDA filings for Pierre Fabre Medical Devices. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3012481408
• FEI Number: 3012481408
• Name: PIERRE FABRE MEDICAL DEVICES
• Owner & Operator: Pierre Fabre Pharmaceuticals, Inc.
• Contact Address: 8 Campus Drive 2nd Floor; Parsippany NJ 07054 US
• Official Correspondent:
  • Kristen Snaguski
  • 01-973-6471640-x
• US Agent:
  • Kristen Snaguski
  • PIERRE FABRE PHARMACEUTICALS, INC.
  • 973 6471640
  • 973 8986573
  • kristen.snaguski@pierre-fabre.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 29 Avenue du Sidobre ; Castres Midi-Pyrenees, 81106 FR
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
PMN K113807 | FRO PIERRE FABRE MEDICAL DEVICES [Pierre Fabre Pharmaceuticals, Inc.]	DEXERYL	2016-10-12
PMN K113807 PIERRE FABRE MEDICAL DEVICES	DEXERYL CREAM	2012-03-07