Speclipse, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Speclipse, Inc. has 2 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Speclipse, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Speclipse, Inc.
2 devices