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Amigo Mobility Intl., Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1821729

Devices
8
Registrations
FDA
FDA recalls
0

What Amigo Mobility Intl., Inc. makes

Amigo Mobility Intl., Inc. manufactures a range of powered mobility devices, including several wheelchair models such as the AMIGO Model 680000 (Excite F 350), AMIGO Wheelchair, AMIGO J-9, AMIGO Model 590000, AMIGO Escort 7.5 (Model 760001 PHS), AMIGO Classic FD, AMIGO RT, and AMIGO Grand Tour.

All of these devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

  • Amigo Model 680000 (Amigo Excite F 350) Ref K992619

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

  • Amigo Wheelchair Ref K010503

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

  • Amigo J-9 Ref K940334

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

  • Amigo Model 590000 Ref K983987

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

  • Amigo Escort 7.5, Model 760001 Phs Ref K092936

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

  • Amigo Classic Fd Ref K101507

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

  • Amigo Rt Ref K981121

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

  • Amigo Grand Tour Ref K952112

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

Company details

FDA FEI number
1821729
Address
6693 DIXIE HWY., BRIDGEPORT, MI, 48722

Frequently asked questions

How many devices does AMIGO MOBILITY INTL., INC. have in the registry?

The registry currently lists 8 devices for AMIGO MOBILITY INTL., INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list AMIGO MOBILITY INTL., INC.'s devices?

Among its 8 most recently registered devices, AMIGO MOBILITY INTL., INC. has devices listed in FDA 510(k) (8 devices).

What risk classes do AMIGO MOBILITY INTL., INC.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for AMIGO MOBILITY INTL., INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from AMIGO MOBILITY INTL., INC. in the registry?

The most recently registered devices listed for AMIGO MOBILITY INTL., INC. include AMIGO MODEL 680000 (AMIGO EXCITE F 350), AMIGO WHEELCHAIR, AMIGO J-9 and AMIGO MODEL 590000.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.