Wen Hao, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wen Hao, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Wen Hao, Inc. has 5 FDA 510(k) cleared medical devices. Based in Pasadena, US.
Historical record: 5 cleared submissions from 1989 to 1990. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Wen Hao, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wen Hao, Inc.
5 devices
Cleared
Jan 24, 1990
PATIENT EXAM GLOVES (MFG JET FAR INDU. INC.)
General Hospital
287d
Cleared
Jan 23, 1990
EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)
General Hospital
286d
Cleared
Jan 19, 1989
DISCARD DENTAL EXPLORER
Dental
31d
Cleared
Jan 19, 1989
DISCARD DENTAL MIRROR
Dental
31d
Cleared
Jan 19, 1989
DENTAL DRESSING PLIERS
Dental
31d