Data / Medical devices / Table, Operating-Room, Ac-Powered / United States
FDA-registered makers of Table, Operating-Room, Ac-Powered in the United States: 25 establishments
25 establishments in the United States are registered with the FDA to make Table, Operating-Room, Ac-Powered (product code FQO). 3 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Table, Operating-Room, Ac-Powered
- Product code
- FQO
- Country
- United States
Makers of Table, Operating-Room, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Steris Corporation | Montgomery, AL, United States | Complaint file establishment, Manufacturer, Manufacturer for export, Repackager or relabeler, Specification developer | 4 | March 20, 2009 | 0 | 0 | 0 | api.fda.gov |
| Moon Surgical, Inc. | San Carlos, CA, United States | Manufacturer | 1 | June 3, 2024 | 0 | 0 | 0 | api.fda.gov |
| voss medical products | San Antonio, TX, United States | Manufacturer | 1 | June 1, 1993 | 0 | 0 | 0 | api.fda.gov |
| Alphatec Spine, Inc. | Carlsbad, CA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amtai Medical Equipment, Inc. | Raleigh, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alphatec Spine, Inc. | Memphis, TN, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Composite Manufacturing, Inc. | San Clemente, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gamamed Vascular Systems Inc. | Loveland, CO, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Herr Enterprises Inc | Jasper, AL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hosmed Inc. | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMRIS Imaging, Inc. | Chaska, MN, United States | Manufacturer | 0 | 0 | 6 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | Spartanburg, SC, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klyo Medical Systems Inc | Doral, FL, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MINDRAY DS USA, Inc. | Mahwah, NJ, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirion Technologies (capintec), Inc | Florham Park, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mizuho Orthopedic Systems, Inc. | Union City, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medrange Corporation | Brea, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirion Technologies (Capintec), Inc. | Meriden, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ondal Medical Systems Of America, Inc. | Sandston, VA, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Opteel Inc. | Airmont, NY, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Medical Technologies- North Manchester Manufacturing Facility | N Manchester, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Tech Services, LLC | Bloomington, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Remington Medical, Inc. | Alpharetta, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STRYKER Communications, Inc. | Flower Mound, TX, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 8 | 0 | api.fda.gov | |
| Skytron, LLC | Grand Rapids, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 6 | 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.