← Every applicant
Erbe Elektromedizin GmbH FDA Approvals
0 new drug approvals and 10 device clearances on file. This applicant is not matched to a listed company.
Newest first
A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.
| Product |
|---|
| ERBECRYO 2 Cryosurgical Unit and Accessories510(k)Jun 9, 2026General, Plastic Surgery |
| ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit; Erbe Flexible Cryoprobe510(k)Apr 22, 2026General, Plastic Surgery |
| MOVIVA® Hybrid Ablation Probe510(k)Dec 18, 2025General, Plastic Surgery |
| Erbe ESU Model VIO® 3n with Accessories510(k)Aug 29, 2025General, Plastic Surgery |
| HybridAPC probe510(k)Jun 20, 2025General, Plastic Surgery |
| FiAPC plus probes510(k)Mar 21, 2025General, Plastic Surgery |
| FiAPC plus probes510(k)Aug 26, 2024General, Plastic Surgery |
| HybridTherm System510(k)Aug 5, 2024General, Plastic Surgery |
| HYBRIDknife® flex510(k)Nov 29, 2023General, Plastic Surgery |
| ERBEJET® 2 System510(k)Jun 15, 2023General Hospital |