Vomaris Wound Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vomaris Wound Care, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Procellera Composite Antibacterial Wound Dressing
1
Total
1
Cleared
0
Denied
Vomaris Wound Care, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tempe, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vomaris Wound Care, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vomaris Wound Care, Inc.
1 devices