Hubdic Co., Ltd. is one of 13011 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hubdic Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Fever Garde, THERMOFINDER, DIGITAL FOREHEAD THERMOMETER, MODEL FS-100
6
Total
6
Cleared
0
Denied
Hubdic Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Historical record: 6 cleared submissions from 2003 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hubdic Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Pharmalink Technical Group, LLC and Plusglobal.
FDA 510(k) Regulatory Record - Hubdic Co., Ltd.
6 devices
Cleared
Dec 18, 2020
Fever Garde
General Hospital
513d
Cleared
Apr 02, 2013
THERMOFINDER
General Hospital
48d
Cleared
Nov 10, 2010
THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301
General Hospital
124d
Cleared
Feb 13, 2009
DUO-MAX BLOOD PRESSURE & GLUCOSE MONITOR HMF-100
Chemistry
344d
Cleared
Mar 04, 2005
DIGITAL FOREHEAD THERMOMETER, MODEL FS-100
General Hospital
92d
Cleared
Apr 09, 2003
THERMO BUDDY, MODELS TB-100, TB-110, TB-120
General Hospital
180d