Lagis Enterprise Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Lagis Enterprise Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LAGIS Endoscopic Instruments- Scissors (EI-330S EI-330S-T EI-330MS EI-330MS-T), LAGIS Suction Irrigation System, LAGIS Endoscopic Instruments - Grasper (DI-5670-33D, DI-5670-45D, DI-5716-33D, DI-5716-45D, DI-5719-33D, DI-5731-33D, DI-5731-45D, DI-5901-33D, DI-5901-45D)
3
Total
3
Cleared
0
Denied
Lagis Enterprise Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Taichung City, TW.
Latest FDA clearance: May 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lagis Enterprise Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lagis Enterprise Co., Ltd.
3 devices
Cleared
May 20, 2026
LAGIS Endoscopic Instruments- Scissors (EI-330S EI-330S-T EI-330MS EI-330MS-T)
General & Plastic Surgery
237d
Cleared
Mar 17, 2025
LAGIS Suction Irrigation System
General & Plastic Surgery
90d
Cleared
Oct 30, 2024
LAGIS Endoscopic Instruments - Grasper (DI-5670-33D, DI-5670-45D,...
General & Plastic Surgery
268d