Bruno Vision Care, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bruno Vision Care, LLC - FDA 510(k) Cleared Devices
Recent clearances: Deseyne (vifilcon C) Daily Disposable Soft (hydrophilic) Contact Lens with UV Blocking for Presbyopia (EDOF), Deseyne (vifilcon C) Daily Disposable Soft (hydrophilic) Contact Lens with UV Blocking for Myopia and Hyperopia
2
Total
2
Cleared
0
Denied
Bruno Vision Care, LLC has 2 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Latest FDA clearance: Dec 2025. Active since 2024. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bruno Vision Care, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Covington & Burling, Llp as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Bruno Vision Care, LLC
2 devices