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Little Wave Arc +1 more model
FDA 510(k)EUDAMEDClass I (US FDA 510(k))
510(k) K223533
Identifiers
- 510(k) Number
- K223533 FDA 510(k)
- FDA Product Code
- LBE FDA 510(k)
- Models / Variants
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 890.3850 FDA 510(k)
- Regulation Number
- 890.3850 FDA 510(k)
- Advisory Committee
- Physical Medicine FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Little Wave Arc +1 more model by Ki Mobility, Llc — Class I — MDR, FDA_510K — listed in FDA 510(k), EUDAMED — 2 models — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
MDR
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Active |
| FDA 510(k) | United States | FDA_510K | K223533 | Class I | Active |
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Manufacturer
- Manufacturer
- Ki Mobility, Llc
Sources (2)
- FDA 510(k) K223533 24 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced May 19, 2026