Bescon Co., Ltd. is one of 25749 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bescon Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: S45 (OCUFILCON A) SPHERICAL, ASPHERICAL, TORIC AND MULTIFOCAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY-, S38 (POLYMACON) SPHERICAL, ASPHERICAL, TORIC AND MULTIFOCAL SOFT CONTACT LENS FOR DAILY WEAR(CLEAR AND TINTED, FULLY-
2
Total
2
Cleared
0
Denied
Bescon Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bescon Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bescon Co., Ltd.
2 devices