Erbe USA, Inc. - FDA 510(k) Cleared Devices
39
Total
39
Cleared
0
Denied
FDA 510(k) cleared devices by Erbe USA, Inc. General & Plastic Surgery ✕
27 devices
Cleared
Oct 27, 2015
ERBE WaterJet Model ERBEJET® 2 System with HybridAPC Probe
General & Plastic Surgery
343d
Cleared
May 04, 2015
ERBECRYO 2 Cryosurgical Unit with accessories
General & Plastic Surgery
14d
Cleared
Dec 11, 2013
ERBE ESU MODEL VIO DV WITH ACCESSORIES
General & Plastic Surgery
55d
Cleared
Jul 16, 2010
ERBE ESU MODEL VIO 100 C WITH ACCESSORIES
General & Plastic Surgery
87d
Cleared
Aug 26, 2009
ERBE HYBRID KNIFE
General & Plastic Surgery
264d
Cleared
Dec 31, 2008
ERBE MODEL VIO 300 D WITH ACCESSORIES
General & Plastic Surgery
40d
Cleared
Apr 02, 2008
ERBE VIO ESU, MODEL VIO 200 S
General & Plastic Surgery
20d
Cleared
Jan 26, 2007
ERBE MONOPOLAR ATTACHMENT FOR HELIX HYDRO-JET, MODEL P/N 20139-094
General & Plastic Surgery
137d
Cleared
Mar 16, 2006
ERBE VIO ESU, MODEL VIO 300 D
General & Plastic Surgery
20d
Cleared
Feb 16, 2006
ERBE BICLAMP OPEN AND LAPAROSCOPIC INSTRUMENTS
General & Plastic Surgery
24d
Cleared
Feb 16, 2006
ERBE APC INTEGRATED FILTER PROBES
General & Plastic Surgery
23d
Cleared
Jul 27, 2005
ERBE ERBOKRYO CA CRYOSURGICAL UNIT & ACCESSORIES
General & Plastic Surgery
50d