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Fusion Core DC Flo - Fusion Core DC Flo
FDA 510(k)Class II (US FDA 510(k))
510(k) K231263
Identifiers
- 510(k) Number
- K231263 FDA 510(k)
- FDA Product Code
- EBF FDA 510(k)
- Models / Variants
- Fusion Core DC Flo FDA 510(k)Fusion Flo FDA 510(k)Fusion Flo SE FDA 510(k)Fusion 1 Seal FDA 510(k)Magna NT FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 872.3690 FDA 510(k)
- Regulation Number
- 872.3690 FDA 510(k)
- Advisory Committee
- Dental FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Fusion Core DC Flo - Fusion Core DC Flo by Prevest Denpro Limited — Class II — FDA_510K — listed in FDA 510(k) — 5 models — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K231263 | Class II | Active |
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Manufacturer
- Manufacturer
- Prevest Denpro Limited
Sources (1)
- FDA 510(k) K231263 24 fields · synced Jun 18, 2026