Data / Medical devices / Chair, Examination And Treatment / United States
FDA-registered makers of Chair, Examination And Treatment in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Chair, Examination And Treatment (product code FRK). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Chair, Examination And Treatment
- Product code
- FRK
- Country
- United States
Makers of Chair, Examination And Treatment 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 | |
| Apramed USA LLC | Kissimmee, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Boyd Industries, Inc. | Clearwater, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Design Specific Us Inc | Wilmington, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JEDMED Instrument Company | Saint Louis, MO, 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, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Professional Specialties Co., Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| REACT Innovations | Charlotte, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Steelcase Inc. | Grand Rapids, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Medical | Portage, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| The Brewer Company LLC | Menomonee Falls, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Metal Fabricators, Inc. | Johnstown, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wieland Designs Inc. | Goshen, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wy'east Medical Corp. | Clackamas, OR, 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.