Data / Medical devices / Freezer / United States
FDA-registered makers of Freezer in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Freezer (product code JRM). 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
- Freezer
- Product code
- JRM
- Country
- United States
Makers of Freezer in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| C Change Surgical LLC | Winston Salem, NC, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Currie Medical, Inc. | Franklin, TN, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Currie Medical, Inc. | Norfolk, VA, United States | Manufacturer, Remanufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Global Cooling, Inc. | Athens, OH, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| HELMER Inc. | Noblesville, IN, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kari Medical | West Orange, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rac Medical Solutions | Bruceton, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| So-Low Environmental Equip. Co.,Inc. | Cincinnati, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thermo Fisher Scientific (asheville) LLC | Marietta, OH, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thermo Fisher Scientific (asheville) LLC | Asheville, NC, United States | Complaint file establishment, Manufacturer | 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.