Data / Medical devices / United States / Bruin Biometrics, LLC
Bruin Biometrics, LLC: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Bruin Biometrics, LLC is registered with the FDA (registration 3009769359) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 20, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009769359
- Address
- 1801 Century Park E Ste 460, Los Angeles, CA, United States, 90067
- Owner or operator
- Bruin Biometrics, LLC (10046475)
- Roles
- Manufacturer, Specification developer
- First device listed
- January 3, 2019
- Registered through
- 2026
- Brand names listed
- Provizio SEM Scanner
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pressure Ulcer Management Tool | QEF | 1 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| December 20, 2018 | DEN170021 | SEM Scanner (Model 200) | QEF | Unknown | Bruin Biometrics, LLC | accessdata.fda.gov |
Compare with other makers
Updated December 20, 2018. 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.