Data / Medical devices / Instrument, Vitreous Aspiration And Cutting, Ac-Powered / United States
FDA-registered makers of Instrument, Vitreous Aspiration And Cutting, Ac-Powered in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Instrument, Vitreous Aspiration And Cutting, Ac-Powered (product code HQE). 9 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 3, 2026.
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- Device
- Instrument, Vitreous Aspiration And Cutting, Ac-Powered
- Product code
- HQE
- Country
- United States
Makers of Instrument, Vitreous Aspiration And Cutting, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medical Instrument Development Laboratories, Inc. | San Leandro, CA, United States | Contract manufacturer, Manufacturer | 3 | April 29, 2016 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 2 | April 29, 2016 | 0 | 3 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Saint Louis, MO, United States | Manufacturer, Repackager or relabeler | 2 | April 29, 2016 | 0 | 1 | 0 | api.fda.gov |
| Alcon Research, LLC | Sinking Spring, PA, United States | Manufacturer | 1 | August 22, 2014 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Lake Forest, CA, United States | Specification developer | 1 | August 22, 2014 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Irvine, CA, United States | Manufacturer | 1 | August 22, 2014 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Houston, TX, United States | Manufacturer | 1 | August 22, 2014 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Manchester, MO, United States | Manufacturer, Repackager or relabeler | 1 | April 29, 2002 | 0 | 0 | 0 | api.fda.gov |
| Synergetics, Inc. | O Fallon, MO, United States | Manufacturer | 1 | February 23, 1994 | 0 | 1 | 0 | api.fda.gov |
| Armm, Inc. | Huntington Beach, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microsurgical Technology, Inc. | Redmond, WA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Peregrine Surgical, LLC. | New Britain, PA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zevex, Inc. | Salt Lake City, UT, 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.