Largan Medical Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Largan U38 Color (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens, “LARGAN Health AI-Tech” Sleep Apnea and Sleep Quality Examination System (ST-SLP03A), Largan DB / DB Color (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens, Largan DB / DB Color (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens for Astigma, Largan DB / DB Color (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens for Presbyo
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Largan Medical Co., Ltd. Anesthesiology ✕
1 devices