Tangible Science, LLC is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tangible Science, LLC - FDA 510(k) Cleared Devices
Recent clearances: Tangible Hydrogel with Tangible Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens, Tangible Hydrogel w/ Hydra-PEG (etafilcon A) Soft (Hydrophilic) Daily Wear Contact Lens
2
Total
2
Cleared
0
Denied
Tangible Science, LLC has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Tangible Science, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tangible Science, LLC
2 devices