Genicon - FDA 510(k) Cleared Devices
Recent clearances: GENISTRONG SINGLE-USE SPECIMEN RETRIEVAL BAG, IMPLANTABLE CLIP, GENICON DISPOSABLE ELECTROSURGICAL INSTRUMENTATION, MODEL 533-005-910
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Genicon General & Plastic Surgery ✕
5 devices
Cleared
Jun 12, 2014
GENISTRONG SINGLE-USE SPECIMEN RETRIEVAL BAG
General & Plastic Surgery
317d
Cleared
Feb 02, 2010
IMPLANTABLE CLIP
General & Plastic Surgery
21d
Cleared
Oct 10, 2006
GENICON DISPOSABLE ELECTROSURGICAL INSTRUMENTATION, MODEL 533-005-910
General & Plastic Surgery
141d
Cleared
Nov 12, 2004
GENICON SUCTION IRRIGATION SYSTEM
General & Plastic Surgery
114d
Cleared
Nov 03, 2004
GENICON BIPOLAR FORCEPS MODEL # 600-005-005
General & Plastic Surgery
105d