Erbe Elektromedizin GmbH - FDA 510(k) Cleared Devices
Recent clearances: ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit, MOVIVA® Hybrid Ablation Probe, Erbe ESU Model VIO® 3n with Accessories
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Erbe Elektromedizin GmbH General & Plastic Surgery ✕
16 devices
Cleared
Jun 09, 2026
ERBECRYO 2 Cryosurgical Unit and Accessories
General & Plastic Surgery
8d
Cleared
Apr 22, 2026
ERBECRYO 2 Cryosurgical Unit and Accessories: ERBECRYO 2 cryosurgical unit
General & Plastic Surgery
205d
Cleared
Dec 18, 2025
MOVIVA® Hybrid Ablation Probe
General & Plastic Surgery
10d
Cleared
Aug 29, 2025
Erbe ESU Model VIO® 3n with Accessories
General & Plastic Surgery
140d
Cleared
Jun 20, 2025
HybridAPC probe
General & Plastic Surgery
263d
Cleared
Mar 21, 2025
FiAPC plus probes
General & Plastic Surgery
134d
Cleared
Aug 26, 2024
FiAPC plus probes
General & Plastic Surgery
45d
Cleared
Aug 05, 2024
HybridTherm System
General & Plastic Surgery
122d
Cleared
Nov 29, 2023
HYBRIDknife® flex
General & Plastic Surgery
145d
Cleared
Jun 15, 2023
ERBEJET® 2 System
General & Plastic Surgery
65d
Cleared
Jan 07, 2020
ERBECRYO 2 Cryosurgical Unit
General & Plastic Surgery
300d
Cleared
Dec 20, 2019
APC 3 Argon Plasma Coagulation Unit, VIO 3 Electrosurgical Unit, FiAPC...
General & Plastic Surgery
226d