Data / Medical devices / Microscope, Surgical, General & Plastic Surgery / United States
FDA-registered makers of Microscope, Surgical, General & Plastic Surgery in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Microscope, Surgical, General & Plastic Surgery (product code FSO). 0 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
- Microscope, Surgical, General & Plastic Surgery
- Product code
- FSO
- Country
- United States
Makers of Microscope, Surgical, General & Plastic Surgery in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blur Product Development | Cary, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Digital Surgery Systems, Inc | Goleta, CA, United States | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Glycocheck Us, LLC | Alpine, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Unify Medical | Cleveland, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viseon, Inc. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Volk Optical Inc. | Mentor, OH, United States | 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.