Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017590240

FEI Number

3017590240

Entity Name

PALLIARE

City/State/Country

Galway, IE

Establishment Address

Palliare, Galway Business Park, Dangan, Galway H91P2DK, IE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Palliare (Owner Number: 10078788)

Owner / Operator Contact Address

Palliare, Galway Business Park, Dangan, Galway, IE-G H91P2DK, IE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K230474

PMA Number

N/A

All Registered Proprietary Names

LAP 300 END 200S LAP 100 EVA15 LAP 200 END 200M EVA15 Erbe ECO2 plus EVA5

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIF	Insufflator, Laparoscopic	Obstetrics/Gynecology	Class 2	884.1730	2020-11-05
HIF	Insufflator, Laparoscopic	Obstetrics/Gynecology	Class 2	884.1730	2025-05-23
FCX	Insufflator, Automatic Carbon-Dioxide For Endoscope	Gastroenterology, Urology	Class 2	876.1500	2023-06-09

Official Correspondent

John O'Dea

US Agent Details

Paul Dryden Business: ProMedic Email: paul.dryden@promedic.cc Phone: (239) 3076061

Related Public Records

Same Entity

Palliare

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3017565103	PALLIARE INC	Oceanside, CA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K981334	Richard Wolf Medical Instruments Corp.	LAPARO CO2-PNEU (AND WITH VIDEO MONITORING)	1998-09-10

Similar Registrations

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1225798	ATC TECHNOLOGIES INC.	Wilmington, MA, US
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE
1320894	CONMED CORPORATION	Utica, NY, US
3001556604	Novanta Medical GmbH	BERLIN, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017590240. Last updated year: 2026. Please use registration number 3017590240 when referencing this establishment in official correspondence.