Synmertex Co, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synmertex Co, Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Synmertex Co, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Rowland Heights, US.
Historical record: 5 cleared submissions from 2003 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Synmertex Co, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synmertex Co, Ltd.
5 devices
Cleared
Aug 14, 2003
DISPOSABLE POWDER FREE VINYL EXAM GLOVES
General Hospital
29d
Cleared
Aug 14, 2003
DISPOSABLE POWDERED VINYL EXAM GLOVES
General Hospital
28d
Cleared
May 23, 2003
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES WHITE COLOR
General Hospital
49d
Cleared
May 23, 2003
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES
General Hospital
45d
Cleared
May 23, 2003
DISPOSABLE POWDERED VINYL SYNTHETIC EXAM GLOVES
General Hospital
39d