Leggero, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leggero, LLC - FDA 510(k) Cleared Devices
Recent clearances: Element Pediatric Wheelchair
1
Total
1
Cleared
0
Denied
Leggero, LLC has 1 FDA 510(k) cleared medical devices. Based in Burnet, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Leggero, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philosopher'S River, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Leggero, LLC
1 devices