Data / Medical devices / United States / Belco. LLC
Belco. LLC: FDA-registered device maker in Eugene, OR, United States, 2 510(k) clearances
Belco. LLC is registered with the FDA (registration 3033708293) in Eugene, OR, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 10, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033708293
- Address
- 440 E Broadway Ste 200, Eugene, OR, United States, 97401
- Owner or operator
- BELCo. LLC (10091428)
- Roles
- Manufacturer
- First device listed
- October 3, 2024
- Registered through
- 2026
- Brand names listed
- NEAT, Sourcerer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automatic Event Detection Software For Polysomnograph With Electroencephalograph | OLZ | 2 | Manufacturer | accessdata.fda.gov |
| Source Localization Software For Electroencephalograph Or Magnetoencephalograph | OLX | 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 |
|---|---|---|---|---|---|---|
| April 10, 2025 | K250058 | NEAT 001 | OLZ | Substantially Equivalent | Brain Electrophysiology Laboratory Company, LLC | accessdata.fda.gov |
| September 27, 2024 | K241513 | Sourcerer | OLX | Substantially Equivalent | Brain Electrophysiology Laboratory Company, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Source Localization Software For Electroencephalograph Or Magnetoencephalograph
- All makers of Automatic Event Detection Software For Polysomnograph With Electroencephalograph
Updated April 10, 2025. 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.