Data / Medical devices / Photocoagulator And Accessories / United States
FDA-registered makers of Photocoagulator And Accessories in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Photocoagulator And Accessories (product code HQB). 8 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Photocoagulator And Accessories
- Product code
- HQB
- Country
- United States
Makers of Photocoagulator And Accessories in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Synergetics, Inc. | O Fallon, MO, United States | Manufacturer | 4 | April 23, 2012 | 0 | 1 | 0 | api.fda.gov |
| Peregrine Surgical, LLC. | New Britain, PA, United States | Manufacturer | 3 | November 14, 2013 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 2 | June 26, 2013 | 0 | 0 | 0 | api.fda.gov |
| Nidek Incorporated | The Colony, TX, United States | Manufacturer | 2 | July 27, 2011 | 0 | 0 | 0 | api.fda.gov |
| Vortex Surgical, Inc. | Saint Charles, MO, United States | Manufacturer | 2 | November 3, 2022 | 0 | 2 | 0 | api.fda.gov |
| Alcon Research, LLC | Sinking Spring, PA, United States | Manufacturer | 1 | October 17, 2011 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Lake Forest, CA, United States | Specification developer | 1 | October 17, 2011 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Irvine, CA, United States | Manufacturer | 1 | October 17, 2011 | 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 | |
| Ophthalmed LLC | Roswell, GA, 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.