Data / Medical devices / United States / BLOXR Solutions LLC
BLOXR Solutions LLC: FDA-registered device maker in Salt Lake City, UT, United States, 3 510(k) clearances
BLOXR Solutions LLC is registered with the FDA (registration 3009688745) in Salt Lake City, UT, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 13, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009688745
- Address
- 2250 S 1300 W Ste C, Salt Lake City, UT, United States, 84119
- Owner or operator
- BLOXR Solutions, LLC (10041003)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 11, 2012
- Registered through
- 2026
- Brand names listed
- BLOXR Radiation Shield, Disposable Radiation Shield, Disposable Radiation Shield - Thyroid Collar, Personnel Protective Shield, ULTRA BLOX X-ray Attenuating Cream, UltraBLOX X-ray Attenuating Cream, XPF Radiation Shield, XPF Radiation Shield (Veterinary)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cream For X-Ray Attenuation | PDK | 2 | Specification developer | accessdata.fda.gov |
| Shield, Protective, Personnel | KPY | 1 | 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 |
|---|---|---|---|---|---|---|
| January 13, 2014 | K133684 | ULTRABLOX | PDK | Substantially Equivalent | Bloxr Corporation | accessdata.fda.gov |
| May 9, 2013 | DEN120022 | X-RAY ATTENUATING CREAM | PDK | Unknown | Bloxr Corporation | accessdata.fda.gov |
| June 24, 2011 | K110900 | DISPOSABLE THYROID COLLAR | KPY | Substantially Equivalent | Bloxr Corporation | accessdata.fda.gov |
Compare with other makers
Updated January 13, 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.