Paneffort, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paneffort, LLC - FDA 510(k) Cleared Devices
Recent clearances: Paneffort AAMI Level 3 Isolation Gown, Paneffort 3-ply Surgical and Procedural Masks
2
Total
2
Cleared
0
Denied
Paneffort, LLC has 2 FDA 510(k) cleared medical devices. Based in Rochester,, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Paneffort, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Freyr Solutions as regulatory consultant.
FDA 510(k) Regulatory Record - Paneffort, LLC
2 devices