Bioland Technology, Ltd. is one of 40 FDA 510(k) medical device manufacturers from Hong Kong in the dataset, ranked by real submission volume.
Bioland Technology, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Bioland G-425-2V Blood Glucose Monitoring System, Bioland G-425-2 Blood Glucose Monitoring System, Infrared Thermometer (model: E201), Digital Thermometer Model T103, T104
8
Total
8
Cleared
0
Denied
Bioland Technology, Ltd. has 8 FDA 510(k) cleared medical devices. Based in North Point, HK.
Last cleared in 2022. Active since 2009.
Browse the FDA 510(k) cleared devices submitted by Bioland Technology, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bioland Technology, Ltd.
8 devices
Cleared
Aug 12, 2022
Bioland G-425-2V Blood Glucose Monitoring System, Bioland G-425-2 Blood...
Chemistry
693d
Cleared
Apr 05, 2022
Infrared Thermometer (model: E201)
General Hospital
197d
Cleared
Mar 31, 2021
Digital Thermometer Model T103, T104
General Hospital
267d
Cleared
Jan 26, 2021
Blood Pressure Monitor
Cardiovascular
119d
Cleared
Oct 02, 2020
Infrared Thermometer Model E127
General Hospital
155d
Cleared
Sep 21, 2020
Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B
Cardiovascular
111d
Cleared
Mar 20, 2020
Bioland Blood Glucose Monitoring System
Chemistry
273d
Cleared
Jan 16, 2009
BIOLAND BLOOD PRESSURE MONITOR
Cardiovascular
35d