Biomerics Nle is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomerics Nle - FDA 510(k) Cleared Devices
Recent clearances: BNLE Hydrophilic Jacketed Peripheral Guidewire, BNLE Access Guidewire
2
Total
2
Cleared
0
Denied
Biomerics Nle has 2 FDA 510(k) cleared medical devices. Based in Brooklyn Park, US.
Latest FDA clearance: May 2024. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biomerics Nle Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medventure Health as regulatory consultant.
FDA 510(k) Regulatory Record - Biomerics Nle
2 devices