Largan Medical Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
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
Largan Medical Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Taichung, TW.
Latest FDA clearance: Feb 2025. Active since 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Largan Medical Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jens Medical Consulting, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Largan Medical Co., Ltd.
8 devices
Cleared
Feb 04, 2025
Largan U38 Color (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens
Ophthalmic
133d
Cleared
Jul 26, 2024
“LARGAN Health AI-Tech” Sleep Apnea and Sleep Quality Examination System...
Anesthesiology
269d
Cleared
Apr 01, 2021
Largan DB / DB Color (ocufilcon D) Daily Wear Soft (hydrophilic) Contact...
Ophthalmic
244d
Cleared
Nov 13, 2018
Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens, Largan U38...
Ophthalmic
48d
Cleared
Nov 01, 2018
Largan 55 UV Color (Ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens
Ophthalmic
49d
Cleared
Jun 29, 2018
Largan 55 UV (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens, Largan...
Ophthalmic
51d
Cleared
Jun 25, 2018
Largan 55 (methafilcon A) Daily Wear Soft (hydrophilic) Contact Lens, Largan...
Ophthalmic
47d
Cleared
Sep 18, 2017
Largan (hioxifilcon A) Daily Wear Soft (hydrophilic) Contact Lens, Largan...
Ophthalmic
231d