Data / Medical devices / Aberrometer, Ophthalmic / United States
FDA-registered makers of Aberrometer, Ophthalmic in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Aberrometer, Ophthalmic (product code NCF). 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
- Aberrometer, Ophthalmic
- Product code
- NCF
- Country
- United States
Makers of Aberrometer, Ophthalmic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alcon Research, LLC | Lake Forest, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Saint Louis, MO, United States | Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ovitz Corporation | Rochester, NY, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tracey Technologies, Corp. | Houston, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vmax Vision Inc. | Longwood, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wavefront Dynamics, Inc. | Albuquerque, NM, 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.