Data / Medical devices / Pump, Infusion, Ophthalmic / United States
FDA-registered makers of Pump, Infusion, Ophthalmic in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Pump, Infusion, Ophthalmic (product code MRH). 7 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
- Pump, Infusion, Ophthalmic
- Product code
- MRH
- Country
- United States
Makers of Pump, Infusion, Ophthalmic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sight Sciences, Inc. | Menlo Park, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 3 | August 4, 2026 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 2 | January 7, 2000 | 0 | 0 | 0 | api.fda.gov |
| New World Medical, Inc. | Rancho Cucamonga, CA, United States | Complaint file establishment, Manufacturer | 2 | February 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Saint Louis, MO, United States | Manufacturer | 1 | November 25, 1996 | 0 | 0 | 0 | api.fda.gov |
| Microsurgical Technology, Inc. | Redmond, WA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | June 8, 2022 | 0 | 0 | 0 | api.fda.gov |
| Nova Eye Inc. | Fremont, CA, United States | Manufacturer | 1 | April 21, 2005 | 0 | 0 | 0 | api.fda.gov |
| Synergetics, Inc. | O Fallon, MO, United States | Specification developer | 1 | January 7, 2000 | 0 | 0 | 0 | api.fda.gov |
| Escalon Medical Corp | New Berlin, WI, United States | Contract 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.