Somnus Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE, SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR, ELECTROSURGICAL GENERATOR, MODEL S1
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Somnus Medical Technologies, Inc. General & Plastic Surgery ✕
16 devices
Cleared
May 30, 2000
SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR...
General & Plastic Surgery
88d
Cleared
May 16, 2000
SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
8d
Cleared
Mar 17, 2000
ELECTROSURGICAL GENERATOR, MODEL S1
General & Plastic Surgery
31d
Cleared
Nov 02, 1998
SOMNOPLASTY SYSTEM, MODELS S2, 1010/2010,2000/1000,1100,3000/30XX/6000, 1200
General & Plastic Surgery
90d
Cleared
Jan 30, 1998
SOMNUS TISSUE COAGULATING ELECTRODE
General & Plastic Surgery
123d
Cleared
Jan 09, 1998
SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE
General & Plastic Surgery
308d
Cleared
Jan 09, 1998
SOMNUS MODEL 30XX DISPOSABLE TRI-NEEDLE COAGULATING ELECTRODE
General & Plastic Surgery
308d
Cleared
Dec 19, 1997
SOMNOPLASTY SYSTEM
General & Plastic Surgery
87d
Cleared
Jul 17, 1997
SOMNOPLASTY SYSTEM
General & Plastic Surgery
87d
Cleared
Jun 24, 1997
SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
47d
Cleared
Jun 18, 1997
BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL
General & Plastic Surgery
105d
Cleared
Apr 09, 1997
SOMNUS MODEL 615 ELECTROSURGICAL GENERATOR(MODEL 615)
General & Plastic Surgery
55d