Luxtec Corp. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Luxtec Corp. has 15 FDA 510(k) cleared medical devices. Based in Sturbridge, US.
Historical record: 15 cleared submissions from 1986 to 1997.
Browse the FDA 510(k) cleared devices submitted by Luxtec Corp. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Nov 21, 1997
LUXSCOPE
Ophthalmic
88d
Cleared
May 21, 1997
TENOSCOPE
Orthopedic
90d
Cleared
May 14, 1997
TENOSNARE
Orthopedic
90d
Cleared
Sep 08, 1995
REDDY ILLUMINATOR
Gastroenterology & Urology
190d
Cleared
Sep 15, 1989
IMS5000 ILLUMINATED LOUPES
General & Plastic Surgery
25d
Cleared
Apr 26, 1989
LUXTEC ACO SERIES 4000 LIGHT SOURCE
Gastroenterology & Urology
72d
Cleared
May 22, 1987
LUXTEC FIBEROPTIC CABLES
Ear, Nose, Throat
198d
Cleared
Jan 14, 1987
FRAZIER SUCTION TUBE
Ear, Nose, Throat
70d
Cleared
Jan 14, 1987
LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS
Ear, Nose, Throat
70d
Cleared
Jan 13, 1987
LUXTEC LIGHT SOURCES
Gastroenterology & Urology
69d
Cleared
Jan 09, 1987
SPECULUM, VAGINAL, METAL FIBEROPTIC
Obstetrics & Gynecology
29d
Cleared
Dec 09, 1986
LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEM
General & Plastic Surgery
34d
Cleared
Nov 19, 1986
LUTEX HEADLIGHT SYSTEMS
General & Plastic Surgery
14d
Cleared
Nov 19, 1986
LUXTEC RETRACTORS, LUXTEC SPECIALTY RETRACTORS
General & Plastic Surgery
14d
Cleared
Nov 17, 1986
LUXTEC LOUPES FOR SURGICAL VISION
General & Plastic Surgery
12d