Data / Medical devices / Vitrectomy, Instrument Cutter / United States
FDA-registered makers of Vitrectomy, Instrument Cutter in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Vitrectomy, Instrument Cutter (product code MLZ). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Vitrectomy, Instrument Cutter
- Product code
- MLZ
- Country
- United States
Makers of Vitrectomy, Instrument Cutter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alcon Research, LLC | Sinking Spring, PA, United States | Manufacturer | 2 | March 22, 2017 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Lake Forest, CA, United States | Specification developer | 2 | March 22, 2017 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Houston, TX, United States | Manufacturer | 2 | March 22, 2017 | 0 | 0 | 0 | api.fda.gov |
| Johnson & Johnson Surgical Vision, Inc. | Irvine, CA, United States | Manufacturer, Specification developer | 1 | October 8, 2008 | 0 | 0 | 0 | api.fda.gov |
| Vista Ophthalmics | Houston, TX, United States | Specification developer | 1 | May 4, 2022 | 0 | 0 | 0 | api.fda.gov |
| Autocam Medical | Kentwood, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Meditec Cataract Technology Inc | Reno, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lake Region Medical | Chaska, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Instrument Development Laboratories, Inc. | San Leandro, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.