Polycore Optical Pte , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Polycore Optical Pte , Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Polycore Optical Pte , Ltd. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1979 to 1983. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Polycore Optical Pte , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Polycore Optical Pte , Ltd.
7 devices
Cleared
Aug 16, 1983
POLYCORE
Ophthalmic
21d
Cleared
Dec 27, 1982
SINGLE VISION POWER LENS
Ophthalmic
137d
Cleared
Dec 27, 1982
KRYPTOX-ROUND SEGMENT BIFOCAL
Ophthalmic
137d
Cleared
Dec 27, 1982
SUNGLASS & SAFETY PLANO LENS
Ophthalmic
137d
Cleared
Dec 27, 1982
VISIOPAL 75
Ophthalmic
126d
Cleared
Dec 27, 1982
POLYCORE
Ophthalmic
126d
Cleared
Feb 26, 1979
LENS, POLYCORE
Ophthalmic
27d