Data / Medical devices / Thailand / Karma Mobility Co Ltd
Karma Mobility Co Ltd: FDA-registered device maker in Amphur Khamtaleso Nakhon Ratchasima, Thailand, 8 510(k) clearances
Karma Mobility Co Ltd is registered with the FDA (registration 3007675960) in Amphur Khamtaleso Nakhon Ratchasima, Thailand. It lists 4 device types. The FDA files 8 510(k) clearances under its listings, the newest dated November 4, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007675960
- Address
- 30 Moo 7 Tambol Khamtaleso, Amphur Khamtaleso Nakhon Ratchasima, Thailand, 30280
- Owner or operator
- KARMA MOBILITY CO LTD (10028791)
- Roles
- Manufacturer
- First device listed
- March 6, 2009
- Registered through
- 2027
- Brand names listed
- VEHICLE, MOTORIZED 3-WHEELED, Wheelchair, Mechanical, Wheelchair, mechanical, Wheelchair, powered, Wheelchair,Mechanical
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stroller, Adaptive | LBE | 1 | Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| November 4, 2025 | K250576 | Flexx Junior (FLX-J00, FLX-J50) | IOR | Substantially Equivalent | Karma Mobility Co, Ltd. | accessdata.fda.gov |
| October 10, 2006 | K062309 | KARMA MANUAL WHEELCHAIR, MODELS S-ERGO 305 AND S-ERGO 105 | IOR | Substantially Equivalent | Karma Medical Products Co., Ltd. | accessdata.fda.gov |
| October 4, 2006 | K062311 | KARMA MANUAL WHEELCHAIR, MODEL BUDGET 800 | IOR | Substantially Equivalent | Karma Medical Products Co., Ltd. | accessdata.fda.gov |
| August 5, 2004 | K041677 | KARMA SCOOTER, MODEL KS-747.2 | INI | Substantially Equivalent | Karma Medical Products Co., Ltd. | accessdata.fda.gov |
| July 23, 2004 | K041678 | KARMA POWER WHEELCHAIR, MODEL KP-25 | ITI | Substantially Equivalent | Karma Medical Products Co., Ltd. | accessdata.fda.gov |
| June 14, 2002 | K021866 | KARMA 800 SERIES MANUAL WHEELCHAIR | IOR | Substantially Equivalent | Vestil Manufacturing Corp. | accessdata.fda.gov |
| March 15, 2002 | K014127 | KARMA DISCOVERY, MODEL KP40 | ITI | Substantially Equivalent | Vestil Manufacturing Corp. | accessdata.fda.gov |
| August 25, 2000 | K002167 | KARMAN WHEELCHAIR | IOR | Substantially Equivalent | Karman Healthcare, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Stroller, Adaptive
- All makers of Vehicle, Motorized 3-Wheeled
- All makers of Wheelchair, Powered
Updated November 4, 2025. 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.