Neuravi L T D

FDA Filings

This page includes the latest FDA filings for Neuravi 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: 3011370111
• FEI Number: 3011370111
• Name: NEURAVI LIMITED
• Owner & Operator: Neuravi Limited
• Contact Address: Block 3 Ballybritt Business Park; Galway IE-G Galway H91K5YD IE
• Official Correspondent:
  • Niall Fox
  • 353-91-394210-1027
• US Agent:
  • Hannah Foley
  • Codman & Shurtleff,Inc
  • 786 4942755
  • HFOLEY1@ITS.JNJ.COM
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Block 3 Ballybrit Business Park; Galway Galway, H91K5YD IE
• Establishment Type: Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
GUDID 10886704081326 NEURAVI LIMITED	Embotrap ET009533	2022-08-05
GUDID 10886704081319 NEURAVI LIMITED	Embotrap ET009521	2022-08-05
GUDID 10886704082743 NEURAVI LIMITED	EMBOGUARD BG8795U	2021-12-30
GUDID 10886704082736 NEURAVI LIMITED	EMBOGUARD BG8785U	2021-12-30
PMN K212340 Neuravi Limited	EMBOGUARD Balloon Guide Catheter	2021-12-17
PMN K212908 Neuravi Ltd.	EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device	2021-10-13
GUDID 10886704082859 NEURAVI LIMITED	EMBOTRAP ET309645	2021-08-13
PMN K211338 Neuravi Limited	EMBOTRAP III Revascularization Device	2021-07-30
GUDID 10886704084570 NEURAVI LIMITED	EMBOTRAP ET309537	2020-07-24
GUDID 10886704082866 NEURAVI LIMITED	EMBOTRAP ET309522	2020-07-24
PMN K193063 Neuravi, Ltd.	EMBOTRAP III Revascularization Device	2020-07-14
PMN K173452 | NRY NEURAVI LIMITED	EMBOTRAP II	2018-05-14
PMN K173452 Neuravi Ltd.	EmboTrap Ll Revascularization Device	2018-05-09