Data / Medical devices / United States / Biosonic Technologies, LLC
Biosonic Technologies, LLC: FDA-registered device maker in Las Vegas, NV, United States, 1 510(k) clearance
Biosonic Technologies, LLC is registered with the FDA (registration 3010872290) in Las Vegas, NV, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 30, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010872290
- Address
- 6370 Annie Oakley Drive, Las Vegas, NV, United States, 89120
- Owner or operator
- Biosonic Technologies, LLC (10046834)
- Roles
- Specification developer
- First device listed
- May 20, 2014
- Registered through
- 2026
- Brand names listed
- Beautiful Image Model 900
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 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 |
|---|---|---|---|---|---|---|
| April 30, 2014 | K130065 | BEAUTIFUL IMAGE FACIAL SCULPTING DEVICE | NFO | Substantially Equivalent | Biosonic Technologies, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 30, 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.