Cortex Technology A P S

FDA Filings

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

FDA Registration(s)

• Registration Number: 9613249
• FEI Number: 3002987034
• Name: Mary J Grove
• Owner & Operator: CORTEX TECHNOLOGY APS
• Contact Address: Plastvaenget 9 --; HADSUND DK-81 Region Nordjylland 9560 DK
• Official Correspondent:
  • Christian S Thomsen
  • 45-98-574100-x
• US Agent:
  • Mary J Grove
  • CYBERDERM INC:
  • 610 3250112 212
  • mjgrove@cyberderm-inc.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 275 New Darlington Rd ; Media, PA 19063 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 05710188039000 Cortex Technology ApS	Dermascan C Ver. 3 USB A0390008	2018-07-06
GUDID 05710188035330 Cortex Technology ApS	DERMASCAN HIGH FREQUENCY ULTRASOUND PROBE G0353309	2018-07-06
GUDID 05710188035316 Cortex Technology ApS	DERMASCAN HIGH FREQUENCY ULTRASOUND PROBE G0353109	2018-07-06
GUDID 05710188035309 Cortex Technology ApS	DERMASCAN HIGH FREQUENCY ULTRASOUND PROBE G0353009	2018-07-06
GUDID 05710188035293 Cortex Technology ApS	DERMASCAN HIGH FREQUENCY ULTRASOUND PROBE G0352909	2018-07-06
GUDID 05710188020022 Cortex Technology ApS	CryoPro mini E0200219	2018-07-06
GUDID 05710188020015 Cortex Technology ApS	CryoPro maxi E0200119	2018-07-06
PMN K983945 | IYO Mary J Grove [CORTEX TECHNOLOGY APS]	DermaScan C Ultrasonic System	2007-11-06
PMN K982280 | GEH Mary J Grove [CORTEX TECHNOLOGY APS]	CryoPro Mini	2007-11-06
PMN K982280 | GEH Mary J Grove [CORTEX TECHNOLOGY APS]	CryoPro Maxi	2007-11-06
PMN K983945 CORTEX TECHNOLOGY APS	CORTEX DERMASCAN C ULTRASONIC SYSTEM	1999-03-17

Related Finance Registrations

NCAGE Code	R3872	CORTEX TECHNOLOGY APS
CAGE Code	R3872	CORTEX TECHNOLOGY APS