Tso3, Inc. is one of 18423 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tso3, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STERIZONE(R) VP4 Sterilizer, STERIZONE VP4 Sterilizer, STERIZONE VP4 Sterilizer
10
Total
10
Cleared
0
Denied
Tso3, Inc. has 10 FDA 510(k) cleared general hospital devices. Based in Fairport, US.
Historical record: 10 cleared submissions from 2006 to 2019.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biotechnology Transfer, LLC and Im3, Inc..
FDA 510(k) Regulatory Record - Tso3, Inc.
10 devices
Cleared
Jul 19, 2019
STERIZONE(R) VP4 Sterilizer
General Hospital
161d
Cleared
May 09, 2018
STERIZONE VP4 Sterilizer
General Hospital
293d
Cleared
Mar 13, 2018
STERIZONE VP4 Sterilizer
General Hospital
102d
Cleared
Jun 30, 2016
STERIZONE Sterilizer
General Hospital
190d
Cleared
Dec 17, 2014
STERIZONE STERILIZER
General Hospital
226d
Cleared
Dec 17, 2014
STERIZONE SELF-CONTAINED BIOLOGICAL INDICATOR
General Hospital
187d
Cleared
Dec 17, 2014
STERIZONE CHEMICAL INDICATOR
General Hospital
176d
Cleared
Dec 02, 2009
TSO3 OZONE STERILIZER, MODEL 125L
General Hospital
267d
Cleared
May 30, 2008
TSO3 OZONE STERILIZATION WRAP
General Hospital
126d
Cleared
Jul 26, 2006
TSO3 OZONE STERILIZER, MODEL 125L
General Hospital
405d