Data / Medical devices / Magnifier, Hand-Held, Low-Vision / United States
FDA-registered makers of Magnifier, Hand-Held, Low-Vision in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Magnifier, Hand-Held, Low-Vision (product code HJF). 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
- Magnifier, Hand-Held, Low-Vision
- Product code
- HJF
- Country
- United States
Makers of Magnifier, Hand-Held, Low-Vision in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ambi, Inc. | Capitola, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Enhanced Vision Systems, Inc. | Huntingtn Bch, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freedom Scientific BLV Group, LLC. | Clearwater, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICU Eyecare Solutions Inc. | Hollister, CA, 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.