Data / Medical devices / Eye, Artificial, Non-Custom / United States
FDA-registered makers of Eye, Artificial, Non-Custom in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Eye, Artificial, Non-Custom (product code HQH). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Eye, Artificial, Non-Custom
- Product code
- HQH
- Country
- United States
Makers of Eye, Artificial, Non-Custom in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eye Prosthetics Of Wisconsin, Inc. | Brookfield, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jardon Eye Prosthetics, Inc. | Southfield, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JUNE R.R. NICHOLS, OCULARIST LTD. d/b/a OCULARISTS Ltd | Des Plaines, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Legrand Assoc. | Broomall, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lights' Prosthetic Eyes, Inc. | Peoria, IL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midwest Eye Laboratories Sioux Falls LLC | Sioux Falls, SD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midwest Eye Laboratories Woodbury LLC | Saint Paul, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midwest Eye Laboratories, Inc. | Rochester, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midwest Eye Laboratories, Inc. | Eau Claire, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ocular Instruments, Inc. | Bellevue, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ocular Prosthetics, Inc. | Los Angeles, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Soper Brothers & Associates | Houston, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Steven R. Young Ocularist, Inc. | Oakland, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Eye Concern, Inc. | Mesa, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thompson Ocular Prosthetics, Inc. | Olmos Park, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.