Data / Medical devices / United States / Amigo Mobility Intl., Inc.
Amigo Mobility Intl., Inc.: FDA-registered device maker in Bridgeport, MI, United States, 4 510(k) clearances
Amigo Mobility Intl., Inc. is registered with the FDA (registration 1821729) in Bridgeport, MI, United States. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 30, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1821729
- Address
- 6693 Dixie Hwy., Bridgeport, MI, United States, 48722
- Owner or operator
- AMIGO MOBILITY INTL., INC. (1821729)
- Roles
- Manufacturer
- First device listed
- September 22, 2016
- Registered through
- 2026
- Brand names listed
- Classic FD, Escort 7.5, HD, RD, RT Express
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Scale, Platform, Wheelchair | INF | 1 | Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 30, 2010 | K101507 | AMIGO CLASSIC FD | INI | Substantially Equivalent | Amigo Mobility Intl., Inc. | accessdata.fda.gov |
| December 4, 2009 | K092936 | AMIGO ESCORT 7.5, MODEL 760001 PHS | ITI | Substantially Equivalent | Amigo Mobility Intl., Inc. | accessdata.fda.gov |
| June 30, 1998 | K981121 | AMIGO RT | INI | Substantially Equivalent | Amigo Mobility Intl., Inc. | accessdata.fda.gov |
| May 6, 1987 | K871391 | AMIGO-A288310 (SCOOTER, COMMUTER CART, 3-WHEELED) | INF | Substantially Equivalent | Amigo Sales, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Scale, Platform, Wheelchair
- All makers of Wheelchair, Powered
- All makers of Vehicle, Motorized 3-Wheeled
Updated July 30, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.