Ding Hwa Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Ding Hwa Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DV-300 Aspirator
5
Total
5
Cleared
0
Denied
Ding Hwa Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Guishan, Taoyuan, TW.
Historical record: 5 cleared submissions from 2008 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ding Hwa Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by V2k Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ding Hwa Co., Ltd.
5 devices
Cleared
Jul 23, 2018
DV-300 Aspirator
General & Plastic Surgery
55d
Cleared
Jun 23, 2014
CLIQ DV-300 ASPIRATOR
General & Plastic Surgery
83d
Cleared
Apr 28, 2014
SUCTION PUMP
General & Plastic Surgery
112d
Cleared
Dec 30, 2013
CLIQ DV-300 ASPIRATOR
General & Plastic Surgery
158d
Cleared
Apr 24, 2008
SPARMAX ASPIRATOR, MODELS TC-2000V ND VC-701
General & Plastic Surgery
113d