Data / Medical devices / Endoilluminator / United States
FDA-registered makers of Endoilluminator in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Endoilluminator (product code MPA). 10 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
- Endoilluminator
- Product code
- MPA
- Country
- United States
Makers of Endoilluminator in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Peregrine Surgical, LLC. | New Britain, PA, United States | Manufacturer | 5 | August 5, 2024 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 3 | September 11, 2015 | 0 | 0 | 0 | api.fda.gov |
| Nova Eye Inc. | Fremont, CA, United States | Manufacturer | 3 | March 30, 2023 | 0 | 0 | 0 | api.fda.gov |
| Synergetics, Inc. | O Fallon, MO, United States | Manufacturer | 3 | January 5, 1996 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Saint Louis, MO, United States | Manufacturer, Specification developer | 2 | May 19, 1998 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Sinking Spring, PA, United States | Manufacturer | 1 | December 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Lake Forest, CA, United States | Specification developer | 1 | December 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Houston, TX, United States | Manufacturer | 1 | December 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Iridex Corporation | San Jose, CA, United States | Manufacturer | 1 | May 20, 1997 | 0 | 0 | 0 | api.fda.gov |
| Iridex Corporation | Mountain View, CA, United States | Manufacturer | 1 | May 20, 1997 | 0 | 0 | 0 | api.fda.gov |
| Katalyst Surgical, LLC | Chesterfield, MO, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vortex Surgical, Inc. | Saint Charles, MO, 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.