Palette Life Sciences is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palette Life Sciences - FDA 510(k) Cleared Devices
Recent clearances: Barrigel Injectable Gel
1
Total
1
Cleared
0
Denied
Palette Life Sciences has 1 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Palette Life Sciences Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Palette Life Sciences
1 devices