Teh Loong Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teh Loong Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Teh Loong Corp. has 3 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 3 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Teh Loong Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Teh Loong Corp.
3 devices
Cleared
Dec 13, 2005
TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW
General Hospital
78d
Cleared
Nov 10, 2005
TEH LOONG POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW
General Hospital
45d
Cleared
Oct 11, 2005
TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE
General Hospital
15d