Surgical Laser Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Laser Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS, SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921, SLT LASERPRO CTH HOLMIUM LASER SYSTEM
51
Total
51
Cleared
0
Denied
Surgical Laser Technologies, Inc. has 51 FDA 510(k) cleared general & plastic surgery devices. Based in Villa Hills, US.
Historical record: 51 cleared submissions from 1985 to 2004.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Laser Technologies, Inc.
51 devices
Cleared
Nov 08, 2004
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS
General & Plastic Surgery
84d
Cleared
Jan 27, 2003
SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL:...
General & Plastic Surgery
90d
Cleared
Jun 14, 2001
SLT LASERPRO CTH HOLMIUM LASER SYSTEM
General & Plastic Surgery
37d
Cleared
Mar 07, 2001
SLT DIFFUSER FIBER
General & Plastic Surgery
61d
Cleared
Mar 15, 1999
HEMOSLEEVE, MODEL 4.0MM, 5.5MM
General & Plastic Surgery
123d
Cleared
Nov 25, 1998
PNEUMATIC CUTTER SYSTEM
Ear, Nose, Throat
85d
Cleared
Aug 27, 1998
SLT BIPOLAR SHEATH
Ear, Nose, Throat
160d
Cleared
Apr 21, 1998
SLT CL MD CONTACT LASER SYSTEM
General & Plastic Surgery
287d
Cleared
Feb 27, 1998
SLT SELECT FIBER DELIVERY SYSTEM AND CONTACT TIPS
General & Plastic Surgery
42d
Cleared
May 16, 1996
SLT FUMICH PROBE GUIDE
General & Plastic Surgery
77d
Cleared
Feb 05, 1996
SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM (MODIFICATION)
General & Plastic Surgery
143d
Cleared
Oct 06, 1995
SLT THERMALITE DIODE LASER SERIES, DIODE 980, 810, 940
General & Plastic Surgery
116d
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