Data / Medical devices / United States / 1800 Contacts, Inc
1800 Contacts, Inc: FDA-registered device maker in Draper, UT, United States, 1 510(k) clearance
1800 Contacts, Inc is registered with the FDA (registration 3011080538) in Draper, UT, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 28, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011080538
- Address
- 261 W Data Drive suite 100, Draper, UT, United States, 84020
- Owner or operator
- 1800 CONTACTS, INC (10055136)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- June 12, 2017
- Registered through
- 2026
- Brand names listed
- D296680, D318239, Express Exam, ExpressExam, Quick Renew, QuickRenew
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chart, Visual Acuity | HOX | 1 | Manufacturer | accessdata.fda.gov |
| Digital Visual Acuity Test | QTO | 1 | Manufacturer | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| April 28, 2011 | K102895 | ONE DAY FLAT PACK | LPL | Substantially Equivalent | Menicon Co, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Digital Visual Acuity Test
- All makers of Chart, Visual Acuity
- All makers of Lenses, Soft Contact, Daily Wear
Updated April 28, 2011. 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.