Data / Medical devices / United States / TANGIBLE SCIENCE Inc
TANGIBLE SCIENCE Inc: FDA-registered device maker in Campbell, CA, United States, 3 510(k) clearances
TANGIBLE SCIENCE Inc is registered with the FDA (registration 3012862899) in Campbell, CA, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 24, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012862899
- Address
- 1055 Florence Way, Campbell, CA, United States, 95008
- Owner or operator
- Tangible Science (10056543)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- December 20, 2017
- Registered through
- 2026
- Brand names listed
- Etafilcon with Tangible Coating (etafilcon A) Soft (Hydrophilic) Daily Wear Contact Lens, Tangible Boost, Tangible Hydrogel with Tangible Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hydrophilic Re-Coating Solution | QMM | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Lens, Contact, (Disposable) | MVN | 2 | Specification developer | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 24, 2020 | DEN200002 | Tangible Boost | QMM | Unknown | Tangible Science, Inc. | accessdata.fda.gov |
| December 13, 2017 | K172692 | Tangible Hydrogel with Tangible Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens | LPL | Substantially Equivalent | Tangible Science, LLC | accessdata.fda.gov |
| October 18, 2017 | K171125 | Tangible Hydrogel w/ Hydra-PEG (etafilcon A) Soft (Hydrophilic) Daily Wear Contact Lens | LPL | Substantially Equivalent | Tangible Science, LLC | accessdata.fda.gov |
Compare with other makers
Updated September 24, 2020. 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.