Laserscope - FDA 510(k) Cleared Devices
60
Total
60
Cleared
0
Denied
Laserscope has 60 FDA 510(k) cleared general & plastic surgery devices. Based in Santa Clara, US.
Historical record: 60 cleared submissions from 1985 to 2006.
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.
FDA 510(k) cleared devices by Laserscope
60 devices
Cleared
Dec 01, 2006
GREENLIGHT HPS SERIES SURGICAL LASER SYSTEM & ACCESSORIES
General & Plastic Surgery
80d
Cleared
Jun 27, 2006
LASERSCOPE GUIDED DELIVERY DEVICE (GDD) CYSTOURETHROSCOPE & ACCESSORIES
Gastroenterology & Urology
15d
Cleared
Mar 30, 2004
GEMINI SURGICAL LASER SYSTEM & ACCESSORIES
General & Plastic Surgery
97d
Cleared
Nov 17, 2003
AURA ISURGICAL LASER SYSTEM & ACCESSORIES
General & Plastic Surgery
332d
Cleared
Jul 02, 2002
LYRA SURGICAL LASER SYSTEM AND ACCESSIORIES (ND:YAG CONFIGURATION)
General & Plastic Surgery
180d
Cleared
May 21, 2001
LYRA SERIES SURGICAL LASER SYSTEM & ACCESSORIES
General & Plastic Surgery
62d
Cleared
May 01, 2001
LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)
General & Plastic Surgery
90d
Cleared
Mar 06, 2001
LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)
General & Plastic Surgery
90d
Cleared
Dec 15, 2000
LYRA SERIES SURGICAL LASER SYSTEM (SL SERIES, ND:YAG CONFIGURATION)
General & Plastic Surgery
66d
Cleared
Mar 08, 2000
ORION SERIES SURGICAL LASER SYSTEM (SL SERIESQ-SWITCHED ND:YAG CONFIGURATION)
General & Plastic Surgery
370d
Cleared
Aug 27, 1999
LYRA SERIES SURGICAL SYSTEM (SL SERIESQ-SWITCHED ND:YAG CONFIGURATION)
General & Plastic Surgery
162d
Cleared
Mar 05, 1999
AURA DYE LASER SYSTEM (ADLS)
General & Plastic Surgery
84d
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