Intelesens L T D

FDA Filings

This page includes the latest FDA filings for Intelesens L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3004418689
• FEI Number: 3004418689
• Name: Ryan Foringer
• Owner & Operator: INTELESENS LIMITED
• Contact Address: 17 HERON ROAD SYDENHAM BUSINESS PARK; BELFAST, NORTHERN IRELAND GB-DOW Down BT3 9LE GB
• Official Correspondent:
  • PATRICIA - PEPPER
  • 44-28-90736829-x
• US Agent:
  • Ryan Foringer
  • S2 Equipment, LLC
  • 240 8883346
  • ryan@stage2innovations.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 7811 Montrose Road Suite 215 ; Potomac, MD 20854 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 15060484630089 INTELESENS LIMITED	ZENSOR	2019-02-07
GUDID 05060484630099 INTELESENS LIMITED	Zensor electrode	2019-01-21
GUDID 15060484630003 INTELESENS LIMITED	ZENSOR	2018-07-06
GUDID 05060484630051 INTELESENS LIMITED	Zensor+ software	2018-07-06
GUDID 05060484630044 INTELESENS LIMITED	Zensoronline software	2018-07-06
GUDID 15060484630010 INTELESENS LIMITED	Zensor electrode	2018-06-14
GUDID 25060484630031 INTELESENS LIMITED	Aingeal 3-patch electrode	2018-03-29
GUDID 05060484630020 INTELESENS LIMITED	Aingeal	2018-03-29
PMN K153275 Intelesens, Ltd.	Aingeal Activity System	2016-02-26
PMN K151027 INTELESENS LIMITED	Zensor System	2015-10-02
MLN Ryan Foringer [INTELESENS LIMITED]	zensor Electrode; zensor Electrode Array.	2014-12-15
MLN Ryan Foringer [INTELESENS LIMITED]	Aingeal Electrode; Aingeal Electrode Array; Aingeal 2-Patch Electrode Array; Aingeal 3-Patch Electrode Array.	2014-12-15
PMN K131000 INTELESENS LIMITED	V-PATCH SYSTEM	2014-01-08
PMN K110015 INTELESENS LIMITED	VITALSENS, AINGEAL, V-POD	2011-05-20