Largent Health, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Largent Health, LLC - FDA 510(k) Cleared Devices
Recent clearances: FiteBac CC OrthoSeal, FiteBac Antimicrobial Cavity Cleanser, FiteBac Cavity Cleanser
3
Total
3
Cleared
0
Denied
Largent Health, LLC has 3 FDA 510(k) cleared medical devices. Based in Marietta, US.
Last cleared in 2021. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Largent Health, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Secure BioMed Evaluations and Secure Biomed Evalutations.
FDA 510(k) Regulatory Record - Largent Health, LLC
3 devices