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Sign in to claim this brandSoliton, Inc.
US
Last updated May 31, 2026
Information
- Country
- US
- Address
- —
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 057015198
Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Resonic | Rapid Acoustic Pulse Device (RAP) GEN-2.2 | FDA UDI | Class II | Active |
| Rapid Acoustic Pulse Device | K201801 | FDA 510(k) | Class II | Active |
| Resonic Rapid Acoustic Pulse Device | K210964 | FDA 510(k) | Class II | Active |
| Rapid Acoustic Pulse Device | K200331 | FDA 510(k) | Class II | Active |
| Soliton Acoustic Wave Device | K190542 | FDA 510(k) | Class II | Active |
| Resonic Rapid Acoustic Pulse Device | K212502 | FDA 510(k) | Class II | Active |
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