Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004920696

FEI Number

3004920696

Entity Name

GLOBAL INTERCONNECT, INC.

City/State/Country

Pocasset, MA, US

Establishment Address

11 JONATHAN BOURNE DR, Pocasset, MA 02559, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Global Interconnect, Inc. (Owner Number: 10050573)

Owner / Operator Contact Address

11 Jonathan Bourne Drive, Pocasset, MA 02559, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Echo-Screen Camino Single Parameter Monitor, Model SPM-1 Multi-Parameter Monitor )MPM) Integra Camino ICP Monitor Integra Licox PtO2 Monitor ATA Cable 36-IN, Algo Pro Silver EEG Cup Electrodes, Pediatric, 6mm Silver, Lead Length 39"(1M), Product Code 019-772100 Silver Chloride EEG Cup Electrodes, 10mm Ag/AgCl, Lead Length 39" (1m), Product Code 019-417600 Silver Chloride EEG Cup Electrodes, 10mm Ag/AgCl, Lead Length 59" (1.5m), Product Code 019-417700 Gold EEG Cup Electrodes, Pediatric, 6mm Gold, Lead Length 39"(1m), Product Code 019-772500 Silver EEG Cup Electrodes, 10mm Silver, Lead Length 39" (1m), Product Code 019-414600 Silver EEG Cup Electrodes, 10mm Silver, Lead Length 59" (1.5m), Product Code 019-414100 Gold EEG Cup Electrodes, 10mm Gold, Lead Length 59"(1.5m), Product Code 019-413900 Gold EEG Cup Electrodes, Pediatric, 6mm Gold, Lead Length 59"(1.5m), Product Code 019-772600 Gold EEG Cup Electrodes, 10mm Gold, Lead Length 39"(1m), Product Code 019-414400 Silver EEG Cup Electrodes, Pediatric, 6mm Silver, Lead Length 59"(1.5m), Product Code 019-772200 Gold EEG Cup Electrodes, 10mm Gold, Lead Length 98"(2.5m), Product Code 019-433800 Remote Pump Controller Multi-Parameter Monitor )MPM) Camino Single Parameter Monitor, Model SPM-1 Integra Camino ICP Monitor Integra Licox PtO2 Monitor ATA 5 V.2 ATA 3 Cable Assembly Camino Single Parameter Monitor, Model SPM-1 Integra Camino ICP Monitor Multi-Parameter Monitor )MPM) Integra Licox PtO2 Monitor MicroPen EVO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GWJ	Stimulator, Auditory, Evoked Response	Neurology	Class 2	882.1900	2024-05-01
GWM	Device, Monitoring, Intracranial Pressure	Neurology	Class 2	882.1620	2015-12-03
GWJ	Stimulator, Auditory, Evoked Response	Neurology	Class 2	882.1900	2024-05-01
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2018-11-16
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2025-04-02
GWM	Device, Monitoring, Intracranial Pressure	Neurology	Class 2	882.1620	2015-12-03
GWJ	Stimulator, Auditory, Evoked Response	Neurology	Class 2	882.1900	2024-05-01
GWJ	Stimulator, Auditory, Evoked Response	Neurology	Class 2	882.1900	2024-05-01
GWM	Device, Monitoring, Intracranial Pressure	Neurology	Class 2	882.1620	2015-12-03
QAI	Powered Microneedle Device	General, Plastic Surgery	Class 2	878.4430	2024-12-12

Official Correspondent

Sarah Nugent

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Global Interconnect, Inc.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K020558	Integra Neurosciences	LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE	2002-03-21
K070612	Top-Rank Health Care Equipment Co., Ltd.	TOP-RANK ADHESIVE ELECTRODE	2007-05-07
K123915	Grass Technologies, an Astro-Med, Inc. Product Gro	DE48-PLUS	2013-04-24
K073532	Technomed Europe	DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES	2008-05-01
K260363	Ceribell, Inc.	Ceribell Brain Monitor Headband	2026-04-03

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0041-05	Linvatec Corp.	2	Ultra Power Burs, Sterile, Single-Use.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004920696. Last updated year: 2026. Please use registration number 3004920696 when referencing this establishment in official correspondence.