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Sign in to claim this brandAesthetics Biomedical
US
Last updated May 23, 2026
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- US
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Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Unknown |
| Vivace Ultra | VERSION 1.0 | FDA UDI | Class II | Active |
| LUDWIG Electrosurgical Device | K221574 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 13, 2020 | Z-0444-2021 | — | terminated | A high frequency output (2 MHz) has not been cleared for distribution in the U.S. |