Motiva USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Motiva USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: Motiva Flora SmoothSilk Tissue Expander, Intraoperative, Single-Use, Sterile, Silicone Breast Sizer Motiva Implant Matrix
2
Total
2
Cleared
0
Denied
Motiva USA, LLC has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2023. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Motiva USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Motiva USA, LLC
2 devices