Gilero, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gilero, LLC - FDA 510(k) Cleared Devices
Recent clearances: UTC 3mL Medication Cartridge, SmartSite Bag 500mL, SmartSite Bag 250 mL, SmartSite Bag 100 mL
2
Total
2
Cleared
0
Denied
Gilero, LLC has 2 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Last cleared in 2023. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gilero, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Gilero, LLC
2 devices