Meris Investment Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meris Investment Group - FDA 510(k) Cleared Devices
Recent clearances: Serena Sleep Night Guard, Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic Mandibular Advancement (EMA)
2
Total
2
Cleared
0
Denied
Meris Investment Group has 2 FDA 510(k) cleared medical devices. Based in Lakeland, US.
Last cleared in 2023. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Meris Investment Group Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medavice, Inc. and Prime Path Medtech.
FDA 510(k) Regulatory Record - Meris Investment Group
2 devices