Freyja Healthcare, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Freyja Healthcare, LLC - FDA 510(k) Cleared Devices
Recent clearances: VereSee Optical Veres Needle and Endoscopic Camera, VereSee Optical Veres Needle System
2
Total
2
Cleared
0
Denied
Freyja Healthcare, LLC has 2 FDA 510(k) cleared medical devices. Based in North Andover, US.
Latest FDA clearance: Oct 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Freyja Healthcare, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Brauer Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Freyja Healthcare, LLC
2 devices