Data / Medical devices / Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Source Localization Software For Electroencephalograph Or Magnetoencephalograph (OLX): 11 FDA-registered makers in 7 countries
11 establishments in 7 countries are registered with the FDA to make Source Localization Software For Electroencephalograph Or Magnetoencephalograph (product code OLX, Class 2, 21 CFR 882.1400). 9 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 25 510(k) clearances under this code, the latest on August 16, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- OLX
- Device class
- 2
- Regulation
- 882.1400
- Medical specialty
- Neurology
Makers by country
| Country | Makers |
|---|---|
| United States | 5 |
| Belgium | 1 |
| Finland | 1 |
| Japan | 1 |
| Australia | 1 |
| Canada | 1 |
| South Korea | 1 |
Makers of Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Clouds of Care NV | Ghent Oost-Vlaanderen, Belgium | Manufacturer | 2 | February 13, 2026 | 0 | 0 | 0 | api.fda.gov |
| Megin OY | Espoo Uusimaa, Finland | Complaint file establishment, Manufacturer | 2 | May 15, 2024 | 0 | 0 | 0 | api.fda.gov |
| Persyst Development LLC | Solana Beach, CA, United States | Complaint file establishment, Manufacturer | 2 | February 13, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ricoh Company, Ltd. | Kanazawa Ishikawa, Japan | Manufacturer | 2 | July 2, 2021 | 0 | 0 | 0 | api.fda.gov |
| Belco. LLC | Eugene, OR, United States | Manufacturer | 1 | September 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| Compumedics Limited | Melbourne Victoria, Australia | Complaint file establishment, Manufacturer | 1 | February 5, 2001 | 0 | 0 | 0 | api.fda.gov |
| Lvis Corporation | Palo Alto, CA, United States | Complaint file establishment, Manufacturer | 1 | May 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Magstim Inc | Eugene, OR, United States | Manufacturer | 1 | December 21, 2010 | 0 | 0 | 0 | api.fda.gov |
| Natus Medical Incorporated Dba Excel-Tech Ltd. (xltek) | OAKVILLE Ontario, Canada | Complaint file establishment, Manufacturer | 1 | December 3, 2010 | 0 | 0 | 0 | api.fda.gov |
| Biogx | Birmingham, AL, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Imedisync Inc. | Gangnam-gu Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 16, 2026. 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.