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City Technology Limited

United KingdomFDA applicant, unverified FDA FEI 3004148997

Devices
15
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What City Technology Limited makes

City Technology Limited manufactures respiratory oxygen sensors, including models such as MOX1, MOX2, MOX3, MOX4, MOX6, MOX9, 6050-0004-110, 6600-1278-600, OXYGEN MEDICELS, and CITICELS.

The company's respiratory oxygen sensors are Class II devices listed in the FDA 510(k) and FDA UDI registries, and the company is based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

Newest first, rows 1-15 of 15

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  • MOX6 AA229-M40

    Listed Registry: GUDID Class:II
  • 6050-0004-110

    Listed Registry: GUDID Class:II
  • 6051-0000-219

    Withdrawn Registry: GUDID Class:II
  • 6600-1278-600

    Listed Registry: GUDID Class:II
  • MOX2 AA829-220

    Listed Registry: GUDID Class:II
  • MOX4 AA829-M20

    Listed Registry: GUDID Class:II
  • 6051-0000-216

    Withdrawn Registry: GUDID Class:II
  • 6051-0000-220

    Withdrawn Registry: GUDID Class:II
  • MOX3 AA829-M10

    Listed Registry: GUDID Class:II
  • MOX1 AA829-210

    Listed Registry: GUDID Class:II
  • MOX9 AAD29-210

    Listed Registry: GUDID Class:II
  • 6051-0000-217

    Withdrawn Registry: GUDID Class:II
  • 6051-0000-218

    Withdrawn Registry: GUDID Class:II
  • 6051-0000-222

    Withdrawn Registry: GUDID Class:II
  • Oxygen Medicels, Citicels Ref K041773

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-15 of 15

Company details

FDA FEI number
3004148997
DUNS number
227246220
Address
WALTON ROAD, PORTSMOUTH Hampshire

Frequently asked questions

How many devices does City Technology Limited have in the registry?

The registry currently lists 15 devices for City Technology Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list City Technology Limited's devices?

Among its 15 most recently registered devices, City Technology Limited has devices listed in FDA 510(k) (1 device) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do City Technology Limited's devices fall under?

Among its 15 most recently registered devices, the classes recorded for City Technology Limited's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from City Technology Limited in the registry?

The most recently registered devices listed for City Technology Limited include MOX6 AA229-M40, 6050-0004-110, 6051-0000-219 and 6600-1278-600.

Generated automatically from registry data and not verified by a human reviewer.