Speclipse, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Speclipse, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PICO SHINING (PICO-K, PICO-K, BELLUS-Q
3
Total
3
Cleared
0
Denied
Speclipse, Inc. has 3 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Latest FDA clearance: May 2026. 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) Regulatory Record - Speclipse, Inc.
3 devices