Sterilox Technologies, Inc. is one of 24820 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterilox Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASHE WOUND CLEANSING SYSTEM, STERILOX LIQUID CHEMICAL STERILANT SYSTEM
2
Total
2
Cleared
0
Denied
Sterilox Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Yardley, US.
Historical record: 2 cleared submissions from 2002 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sterilox Technologies, Inc. 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 - Sterilox Technologies, Inc.
2 devices