Vaporox, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Vaporox, Inc. has 2 FDA 510(k) cleared medical devices. Based in Centennial, US.
Latest FDA clearance: Mar 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vaporox, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hyman, Phelps & McNamara, P.C. as regulatory consultant.
FDA 510(k) Regulatory Record - Vaporox, Inc.
2 devices