Data / Medical devices / Aid, Surgical, Viscoelastic / United States
FDA-registered makers of Aid, Surgical, Viscoelastic in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Aid, Surgical, Viscoelastic (product code LZP). 6 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
- Aid, Surgical, Viscoelastic
- Product code
- LZP
- Country
- United States
Makers of Aid, Surgical, Viscoelastic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 0 | 4 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 0 | 3 | 0 | 0 | api.fda.gov | |
| Johnson & Johnson Surgical Vision, Inc. | Irvine, CA, United States | Manufacturer, Specification developer | 0 | 2 | 1 | 0 | api.fda.gov | |
| Anika Therapeutics, Inc. | Bedford, MA, United States | Contract manufacturer, Manufacturer | 0 | 1 | 2 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Clearwater, FL, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Nordic Pharma, Inc. | Berwyn, PA, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Cima Technology, Inc. | Pittsburgh, PA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eyekon Medical, Inc. | Clearwater, FL, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifecore Biomedical LLC | Chaska, MN, United States | Contract manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oasis Medical, Inc. | Glendora, CA, United States | Contract manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Tech Services, LLC | Bloomington, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| U.S. Iol, Inc. | Lexington, KY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visionary Medical Supplies, Inc. | Madison, WI, United States | Manufacturer for export, Specification developer | 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.