Data / Medical devices / United States / Curative Sound Therapeutics, Inc.
Curative Sound Therapeutics, Inc.: FDA-registered device maker in Carmel, IN, United States, 1 510(k) clearance
Curative Sound Therapeutics, Inc. is registered with the FDA (registration 3039142471) in Carmel, IN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 2, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039142471
- Address
- 11611 N Meridian St Ste 425, Carmel, IN, United States, 46032
- Owner or operator
- Curative Sound Therapeutics, Inc. (10093872)
- Roles
- Manufacturer
- First device listed
- July 25, 2025
- Registered through
- 2026
- Brand names listed
- CS-Pro MED
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers | PZL | 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 |
|---|---|---|---|---|---|---|
| July 2, 2025 | K250779 | CS-Pro MED | PZL | Substantially Equivalent | Curative Sound Therapeutics | accessdata.fda.gov |
Compare with other makers
Updated July 2, 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.