Confortex S A

FDA Filings

This page includes the latest FDA filings for Confortex S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3001159036
• FEI Number: 3001159036
• Name: DENNIS CASE
• Owner & Operator: CONFORTEX, S.A.
• Contact Address: del la escuela publica de Guachipelin de Escazu 200mts norte y 75 mts oeste; SAN JOSE CR-SJ San Jose 0 CR
• Official Correspondent:
  • ALVARO SANCHO
  • 506-2228-4992-x
• US Agent:
  • DENNIS CASE
  • PEDIFIX, INC.
  • 845 2772850
  • 845 2772851
  • dennis.case@pedifix.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 301 FIELDS LN ; Brewster, NY 10509 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
IQM DENNIS CASE [CONFORTEX, S.A.]	PEDIFIX TOE STRAIGHTENER	2012-12-31
IQM DENNIS CASE [CONFORTEX, S.A.]	PEDIFIX BUDIN SPLINT	2012-12-31