Sterilucent, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sterilucent, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sterilucent self-Contained Biological Indicator, Sterilucent Lumen Cycle Process Challenge Device, Sterilucent Flexible Cycle Process Challenge Device, Sterilucent VH2O2 Chemical Indicators, Sterilucent HC 80TT Hydrogen Peroxide Sterilizer
7
Total
7
Cleared
0
Denied
Sterilucent, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 2014 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sterilucent, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sterilucent, Inc.
7 devices
Cleared
Oct 22, 2019
Sterilucent self-Contained Biological Indicator, Sterilucent Lumen Cycle...
General Hospital
88d
Cleared
Oct 21, 2019
Sterilucent VH2O2 Chemical Indicators
General Hospital
87d
Cleared
Sep 13, 2019
Sterilucent HC 80TT Hydrogen Peroxide Sterilizer
General Hospital
254d
Cleared
Jan 20, 2015
STERILUCENT STERILIZATION CONTAINER SYSTEM
General Hospital
169d
Cleared
Nov 03, 2014
STERILUCENT SELF-CONTAINED BIOLOGICAL INDICATOR
General Hospital
174d
Cleared
Oct 31, 2014
STERILUCENT PSD-85 HYDROGEN PEROXIDE STERILIZER
General Hospital
249d
Cleared
Oct 31, 2014
STERILUCENT PROCESS CHALLENGE DEVICE
General Hospital
164d