Data / Medical devices / Unit, Drying / United States
FDA-registered makers of Unit, Drying in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Unit, Drying (product code JRJ). 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
- Unit, Drying
- Product code
- JRJ
- Country
- United States
Makers of Unit, Drying 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 | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Capsa Healthcare | Canal Winchester, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cenorin, LLC | Kent, WA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| MG Development America Inc. | Pittsburgh, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sheldon MFG., Inc. | Cornelius, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wassenburg Medical, Inc. | Ivyland, PA, United States | Manufacturer, 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.