Sandstone Medical Technologies, LLC is one of 20342 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sandstone Medical Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: POLARIS Q-SWITCH RUBY SYSTEM, CORTEX CO2 / ER:YAG LASER SYSTEM, TRIPLEX ER. YAG / ND: YAG SYSTEM
11
Total
11
Cleared
0
Denied
Sandstone Medical Technologies, LLC has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Woodland, US.
Historical record: 11 cleared submissions from 2004 to 2012.
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) Regulatory Record - Sandstone Medical Technologies, LLC
11 devices
Cleared
Jul 18, 2012
POLARIS Q-SWITCH RUBY SYSTEM
General & Plastic Surgery
92d
Cleared
Jul 01, 2011
CORTEX CO2 / ER:YAG LASER SYSTEM
General & Plastic Surgery
93d
Cleared
Apr 27, 2011
TRIPLEX ER. YAG / ND: YAG SYSTEM
General & Plastic Surgery
64d
Cleared
Apr 08, 2011
APEX ER. YAG / IPL SYSTEM
General & Plastic Surgery
65d
Cleared
Jun 16, 2010
CHEVEUX DIODE LASER SYSTEM
General & Plastic Surgery
77d
Cleared
Feb 18, 2010
LS-40 CO2 LASER SYSTEM MODEL LS-40
General & Plastic Surgery
70d
Cleared
Feb 03, 2009
MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEM
General & Plastic Surgery
166d
Cleared
Nov 05, 2008
LS FAMILY OF CO2 LASERS WITH SCANNING HANDPIECE
General & Plastic Surgery
103d
Cleared
Jun 30, 2008
APOLLO MINI IPL SYSTEM
General & Plastic Surgery
61d
Cleared
Dec 14, 2004
ULTRALIGHT II ND:YAG LASER SYSTEM
General & Plastic Surgery
238d
Cleared
Oct 08, 2004
LS FAMILY OF CO2 LASERS INCLUDING: LS-15 LASER SYSTEM (15 WATT) AND LS-25...
General & Plastic Surgery
219d