Data / Medical devices / Singapore / Clearlab SG Pte, Ltd.
Clearlab SG Pte, Ltd.: FDA-registered device maker in SINGAPORE South East, Singapore, 5 510(k) clearances
Clearlab SG Pte, Ltd. is registered with the FDA (registration 9614154) in SINGAPORE South East, Singapore. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 15, 2008. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 9614154
- FEI number
- 3001064204
- Address
- 139 Joo Seng RD., SINGAPORE South East, Singapore, 368362
- Owner or operator
- CLEARLAB SG PTE LTD. (9033539)
- Roles
- Manufacturer
- First device listed
- April 9, 1998
- Registered through
- 2026
- Brand names listed
- Preferred 55, clear55A, clear55A UV, clear58, clearall-day, clearall-day T, eyedia fresh daily disposable, eyedia percise monthly for astigmatism and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lens, Contact, (Disposable) | MVN | 2 | Manufacturer | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 15, 2008 | K080632 | CLEAR1-DAY HIOXIFILCON DAILY DISPOSABLE SOFT CONTACT LENS | MVN | Substantially Equivalent | Clearlab SG Pte, Ltd. | accessdata.fda.gov |
| May 15, 2006 | K052290 | AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS | LPL | Substantially Equivalent | Clearlab Pte , Ltd. | accessdata.fda.gov |
| April 2, 2003 | K030167 | MIERU (ETAFILCON A) DAILY WEAR CONTACT LENS CLEAR AND VISIBILITY TINT, WITH UV BLOCKER | LPL | Substantially Equivalent | Clearlab Pte , Ltd. | accessdata.fda.gov |
| June 4, 2002 | K020855 | IGEL 55UV (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IGEL 55 UV MULTIFOCAL (METHAFILCON A) SOFT | LPL | Substantially Equivalent | Igel Vision Care Pte , Ltd. | accessdata.fda.gov |
| February 13, 2001 | K003833 | SPECIALTY 55 & MULTIFOCAL (METHAFILCON A) SOFT (HYDROPHILIC CONTACT LENSES FOR DAILY WEAR | LPL | Substantially Equivalent | Clearlab Pte , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 15, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.