Clearlab Pte , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clearlab Pte , Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Clearlab Pte , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 4 cleared submissions from 2001 to 2006. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Clearlab Pte , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clearlab Pte , Ltd.
4 devices
Cleared
May 15, 2006
AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS
Ophthalmic
265d
Cleared
May 14, 2003
AQUASOFT (OCUFILCON D) DAILY WEAR CONTACT LENS CLEAR AND VISIBILITY TINT,...
Ophthalmic
65d
Cleared
Apr 02, 2003
MIERU (ETAFILCON A) DAILY WEAR CONTACT LENS CLEAR AND VISIBILITY TINT, WITH...
Ophthalmic
76d
Cleared
Feb 13, 2001
SPECIALTY 55 & MULTIFOCAL (METHAFILCON A) SOFT (HYDROPHILIC CONTACT LENSES...
Ophthalmic
64d