Single Pass, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Single Pass, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Single Pass, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Geissinger Regulatory Consulting, Inc. as regulatory consultant.
2 devices