Data / Medical devices / Conformer, Ophthalmic / United States
FDA-registered makers of Conformer, Ophthalmic in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Conformer, Ophthalmic (product code HQN). 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
- Conformer, Ophthalmic
- Product code
- HQN
- Country
- United States
Makers of Conformer, Ophthalmic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Armm, Inc. | Huntington Beach, CA, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Manchester, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dallas Eye Prosthetics | Dallas, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gulden Ophthalmics | Elkins Park, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Integrated Orbital Implants, Inc. | San Diego, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jardon Eye Prosthetics, Inc. | Southfield, MI, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Katena Products, Inc. | Parsippany, NJ, United States | Specification developer | 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 | |
| Millstone Medical Outsourcing LLC. | Fall River, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Retivue LLC | Charlottesville, VA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Soper Brothers & Associates | Houston, 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.