Data / Medical devices / United States / DMX Imaging, LLC
DMX Imaging, LLC: FDA-registered device maker in Palm Harbor, FL, United States, 1 510(k) clearance
DMX Imaging, LLC is registered with the FDA (registration 1000221974) in Palm Harbor, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 27, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000221974
- Address
- 4159 Coprorate Court Suite B, Palm Harbor, FL, United States, 34683
- Owner or operator
- DMX Works Imaging, Inc (10039116)
- Roles
- Manufacturer
- First device listed
- December 9, 2011
- Registered through
- 2026
- Brand names listed
- John Postlethwaite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, X-Ray, Fluoroscopic, Image-Intensified | JAA | 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 |
|---|---|---|---|---|---|---|
| December 27, 1994 | K943272 | VISUALIZER 2000 | JAA | Substantially Equivalent | Vf-Works, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 27, 1994. 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.