Data / Medical devices / United States / Sonorous NV, Inc.
Sonorous NV, Inc.: FDA-registered device maker in Lake Forest, CA, United States, 1 510(k) clearance
Sonorous NV, Inc. is registered with the FDA (registration 3047894544) in Lake Forest, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 21, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3047894544
- Address
- 1 Spectrum Pointe Dr. Suite 150, Lake Forest, CA, United States, 92630
- Owner or operator
- Sonorous NV, Inc. (10096089)
- Roles
- Specification developer
- First device listed
- June 23, 2026
- Registered through
- 2026
- Brand names listed
- BosCATH Support Catheter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous | DQY | 2 | Specification developer | accessdata.fda.gov |
| Catheter, Percutaneous, Neurovasculature | QJP | 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 21, 2026 | K254046 | BosCATH Support Catheter | QJP | Substantially Equivalent | Sonorous NV, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 21, 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.