CLEARLAB SG PTE. LTD.
US Last updated 25 May 2026
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- Devices
- 14
- Registries
- GUDIDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
clear1-day Multifocal Ref clear1-day Multifocal
clearall-day Ref clearall-day
clear55A Ref clear55A
clearall-day Toric Ref clearall-day Toric
clear55AUV Ref clear55AUV
clear1-day Ref clear1-day
clear1-day Toric Ref clear1-day Toric
clear58 Ref clear58
FDA establishments
- Clearlab Sg Pte, Ltd. SINGAPORE South East · SG FEI 3001064204
What CLEARLAB SG PTE. LTD. makes
ClearLab SG Pte. Ltd. manufactures soft corrective contact lenses for daily wear and daily disposable use, including multifocal, toric, and colored variants made from materials such as hioxifilcon A.
These devices are classified as Class II medical devices and are listed in the FDA’s 510(k) and UDI registries; the company is based in the United States.
Frequently asked questions
What type of medical devices does ClearLab SG Pte. Ltd. manufacture?
ClearLab SG Pte. Ltd. manufactures soft corrective contact lenses designed for daily wear and daily disposable use, including multifocal, toric, and colored variants made from materials such as hioxifilcon A, which are intended to correct vision.
Where is ClearLab SG Pte. Ltd. based?
ClearLab SG Pte. Ltd. is based in the United States, as indicated in the company's country of registration within the provided device data.
In which regulatory registries are ClearLab SG Pte. Ltd.'s devices listed?
The devices manufactured by ClearLab SG Pte. Ltd. are listed in the FDA’s 510(k) and UDI registries, which are used to track medical device submissions and unique device identifiers for traceability and oversight.
How are ClearLab SG Pte. Ltd.'s contact lenses classified as medical devices?
ClearLab SG Pte. Ltd.'s soft corrective contact lenses are classified as Class II medical devices, indicating they require special controls to ensure safety and effectiveness, but do not undergo the most stringent premarket approval process.
Information
- Country
- US
- DUNS number
- 595115032