Appliedvr is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Appliedvr - FDA 510(k) Cleared Devices
Recent clearances: RelieVRx (Pico G3), RelieVRx
2
Total
2
Cleared
0
Denied
Appliedvr has 2 FDA 510(k) cleared medical devices. Based in Van Nuys, US.
Latest FDA clearance: Aug 2025. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Appliedvr Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Appliedvr
2 devices