Data / Medical devices / United States / Driving Force Vma, LLC
Driving Force Vma, LLC: FDA-registered device maker in Broussard, LA, United States, 3 510(k) clearances
Driving Force Vma, LLC is registered with the FDA (registration 3042625805) in Broussard, LA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated January 17, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042625805
- Address
- Driving Force Company 3827 Pinhook Rd, Broussard, LA, United States, 70518
- Owner or operator
- Driving Force VMA, LLC (10094822)
- Roles
- Specification developer
- First device listed
- December 30, 2025
- Registered through
- 2026
- Brand names listed
- VMA (Vertebral Motion Analyzer), VMA (Vertebral Motion Analyzer) Version 1.1, VMA (Vertebral Motion Analyzer) Version 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| January 17, 2014 | K133875 | THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.2, THE MOTION NORMALIZER PATIENT HANDLING AND DATA | LLZ | Substantially Equivalent | Ortho Kinematics, Inc. | accessdata.fda.gov |
| August 6, 2013 | K130743 | THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLL | LLZ | Substantially Equivalent | Ortho Kinematics, Inc. | accessdata.fda.gov |
| December 22, 2011 | K112109 | THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLECTION DEVICE | LLZ | Substantially Equivalent | Ortho Kinematics, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 17, 2014. 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.