Clearlab SG Pte, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clearlab SG Pte, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ClearColor 1-day (hioxifilcon A) Daily Disposable Soft (hydrophilic) Contact Lens, Aryan Color 1-day (hioxifilcon A) Daily Disposable Soft (hydrophilic) Contact Lens
2
Total
2
Cleared
0
Denied
Clearlab SG Pte, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 2 cleared submissions from 2008 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Clearlab SG Pte, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Clearlab Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Clearlab SG Pte, Ltd.
2 devices