Data / Medical devices / Warmer, Blood, Non-Electromagnetic Radiation / United States
FDA-registered makers of Warmer, Blood, Non-Electromagnetic Radiation in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Warmer, Blood, Non-Electromagnetic Radiation (product code BSB). 5 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
- Warmer, Blood, Non-Electromagnetic Radiation
- Product code
- BSB
- Country
- United States
Makers of Warmer, Blood, Non-Electromagnetic Radiation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Belmont Medical Technologies | Billerica, MA, United States | Manufacturer | 2 | November 16, 2011 | 0 | 0 | 0 | api.fda.gov |
| Estill Medical Technologies, Inc. | Dallas, TX, United States | Specification developer | 2 | July 26, 2001 | 0 | 1 | 0 | api.fda.gov |
| Solventum Us LLC | Eagan, MN, United States | Specification developer | 1 | April 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Solventum US LLC | San Antonio, TX, United States | Complaint file establishment, Specification developer | 1 | April 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Solventum US LLC | Eden Prairie, MN, United States | Manufacturer, Repackager or relabeler | 1 | April 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Garrett Heilbrun Technology Partners, LLC Dba Cobalt Product Solutions | Plano, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Icu Medical, Inc. | Lake Forest, IL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Contract 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.