Data / Medical devices / Chair, Surgical, Ac-Powered / United States
FDA-registered makers of Chair, Surgical, Ac-Powered in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Chair, Surgical, Ac-Powered (product code GBB). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Chair, Surgical, Ac-Powered
- Product code
- GBB
- Country
- United States
Makers of Chair, Surgical, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Champion MFG, INC. | Ocala, FL, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Dentronic | San Leandro, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dexta Corp. | Napa, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GF Health Products, Inc | Atlanta, GA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GF Health Products, Inc. | Fond du Lac, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JEDMED Instrument Company | Saint Louis, MO, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Knu, LLC | Leland, MS, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Knu, LLC | Cannelton, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Technology Industries, Inc. | Salt Lake City, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midmark Corporation | Versailles, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schuerch Corporation | Abington, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smart Step Surgical, LLC | Billings, MT, United States | 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.