Freyja Healthcare, LLC is one of 16115 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 (VER150, VER200, VER151, VER201, VER200C, and VER-100-103), VereSee Optical Veres Needle and Endoscopic Camera, VereSee Optical Veres Needle System
3
Total
3
Cleared
0
Denied
Freyja Healthcare, LLC has 3 FDA 510(k) cleared medical devices. Based in North Andover, US.
Latest FDA clearance: Aug 2026. 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
3 devices
Cleared
Aug 13, 2026
VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)
General & Plastic Surgery
128d
Cleared
Oct 20, 2025
VereSee Optical Veres Needle and Endoscopic Camera
General & Plastic Surgery
60d
Cleared
May 02, 2024
VereSee Optical Veres Needle System
Obstetrics & Gynecology
261d