Medical Device Manufacturer · US , Bridgeport , MI

Amigo Mobility Intl., Inc. - FDA 510(k) Cleared Devices

8 submissions · 7 cleared · Since 1994

Total

Cleared

Denied

Amigo Mobility Intl., Inc. has 7 FDA 510(k) cleared medical devices. Based in Bridgeport, US.

Historical record: 7 cleared submissions from 1994 to 2010. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Amigo Mobility Intl., Inc. Filter by specialty or product code using the sidebar.

Amigo Mobility Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Amigo Mobility Intl., Inc.

8 devices

1-8 of 8

Cleared Jul 30, 2010

AMIGO CLASSIC FD

K101507 · INI

Physical Medicine · 59d

Cleared Dec 04, 2009

AMIGO ESCORT 7.5, MODEL 760001 PHS

K092936 · ITI

Physical Medicine · 71d

Cleared Jul 06, 2001

AMIGO WHEELCHAIR

K010503 · INI

Physical Medicine · 135d

Cleared Oct 25, 1999

AMIGO MODEL 680000 (AMIGO EXCITE F 350)

K992619 · ITI

Physical Medicine · 82d

Cleared Jun 08, 1999

AMIGO MODEL 590000

K983987 · INI

Physical Medicine · 211d

Cleared Jun 30, 1998

AMIGO RT

K981121 · INI

Physical Medicine · 95d

Cleared Aug 11, 1995

AMIGO GRAND TOUR

K952112 · INI

Physical Medicine · 98d

Cleared May 18, 1994

AMIGO J-9

K940334 · INI

Physical Medicine · 113d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Amigo Mobility Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Amigo Mobility Intl., Inc.

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