Xtrallux, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xtrallux, LLC - FDA 510(k) Cleared Devices
Recent clearances: Xtrallux Alpha (XA136R-USA), Xtrallux Super Plus (XS276R-USA/XS276L-USA), Xtrallux Turbo Pro (XP316R-USA), Xtrallux Extreme RX (XR352R-USA)
1
Total
1
Cleared
0
Denied
Xtrallux, LLC has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Xtrallux, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Xtrallux, LLC
1 devices