CITY TECHNOLOGY LIMITED

FDA Device Registration & Listing · PORTSMOUTH Hampshire, GB · Registration 3004148997

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004148997
FEI Number
3004148997
Entity Name
CITY TECHNOLOGY LIMITED
City/State/Country
PORTSMOUTH Hampshire, GB
Establishment Address
WALTON ROAD, PORTSMOUTH Hampshire PO6 1SZ, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
CITY TECHNOLOGY (Owner Number: 9058534)
Owner / Operator Contact Address
WALTON ROAD, --, PORTSMOUTH, GB-POR PO6 1SZ, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MOX1 MOX4 MOX3 MOX2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCL Analyzer, Gas, Oxygen, Gaseous-Phase Anesthesiology Class 2 868.1720 2007-12-10

Official Correspondent

Keith Johnson

US Agent Details

Stephen Gorski Business: Imagenix, Inc. Email: stephengorski@me.com Phone: (414) 7374596

Related Public Records

Same Entity

CITY TECHNOLOGY
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
K072469 Digiflo, Inc. DIGIFLO CONCENTRATOR ANALYZER 2008-01-03

Similar Registrations

Registration Number Establishment Name Location
1062836 DIGICARE BIOMEDICAL TECHNOLOGY, INC. BOYNTON BEACH, FL, US
2026424 Teledyne Analytical Instruments City Industry, CA, US
9613449 IT DR. GAMBERT GMBH WISMAR Mecklenburg-Western Pomerania, DE
3009156722 SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. Shenzhen Guangdong, CN
3004415070 KB Components Finland Oy Nurmijarvi Etela-Karjala, FI
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004148997. Last updated year: 2026. Please use registration number 3004148997 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.