Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011632150

FEI Number

3011632150

Entity Name

VERYAN MEDICAL LIMITED

City/State/Country

Galway, IE

Establishment Address

Block 5, Parkmore East Business Park, Galway Technology Park, Parkmore, Galway H91 V0TX, IE

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Veryan (Owner Number: 10058865)

Owner / Operator Contact Address

Block 5, Parkmore East Business Park, Block 5, Galway Technology Park, Parkmore, Galway, IE-G H91 V0TX, IE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P180003

All Registered Proprietary Names

BioMimics 3D Vascular Stent System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NIP	Stent, Superficial Femoral Artery	Unknown	Class 3	N/A	2018-11-04

Official Correspondent

Martha Folan

US Agent Details

Semih Oktay Business: CardioMed Device Consultants LLC Email: soktay@cardiomedllc.com Phone: (410) 6742060

Related Public Records

Same Entity

Veryan

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2014	Bard Peripheral Vascular Inc	3	Bard LifeStent Solo Vascular Stent, Item Numbers: EX062001CL, EX072001CL, EX062003CL, EX072003CL. The LifeStent Solo Vascular Stent System is intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 240 mm in length in the native superficial femoral artery (SFA) and in the proximal popliteal artery with reference vessel diameters ranging from 4.0 6.5 mm.

Similar Registrations

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2134265	BOSTON SCIENTIFIC CORPORATION	Maple Grove, MN, US
2011171	Sterigenics US LLC	Los Angeles, CA, US
3006946276	MEDISTRI SA	Domdidier Fribourg, CH

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011632150. Last updated year: 2026. Please use registration number 3011632150 when referencing this establishment in official correspondence.