Data / Medical devices / Pupillometer, Ac-Powered / United States
FDA-registered makers of Pupillometer, Ac-Powered in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Pupillometer, Ac-Powered (product code HLG). 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
- Pupillometer, Ac-Powered
- Product code
- HLG
- Country
- United States
Makers of Pupillometer, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Brightlamp, Inc | Indianapolis, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diagnosys LLC | Lowell, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heru, Inc. | Miami, FL, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medneuroptek Inc. | Johns Creek, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuroptics, Inc. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nidek Incorporated | The Colony, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Olleyes, Inc. | Summit, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ray Vision Inc. | Lake Forest, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solvemed Inc. | Lewes, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Veero Analytics, LLC | Cambridge, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Walmart Inc. | Bentonville, AR, 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.