Data / Medical devices / Cabinet, Table And Tray, Anesthesia / United States
FDA-registered makers of Cabinet, Table And Tray, Anesthesia in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Cabinet, Table And Tray, Anesthesia (product code BRY). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Cabinet, Table And Tray, Anesthesia
- Product code
- BRY
- Country
- United States
Makers of Cabinet, Table And Tray, Anesthesia in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alimed, LLC | Dedham, MA, United States | Complaint file establishment, Contract manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caf Medical Solutions Inc | Hockley, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Capsa Healthcare | Canal Winchester, OH, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CareFusion 303, INC | San Diego, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 2 | 0 | api.fda.gov | |
| CareFusion 303, INC. | San Diego, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 37 | 0 | api.fda.gov | |
| General Hospital Supply Corp. | Indian Trail, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hosmed Inc. | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intermetro Industries Corp | Wilkes Barre, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iroquois Industrial Group, LLC d.b.a T & D METAL PRODUCTS | Watseka, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Millstone Medical Outsourcing LLC | Olive Branch, MS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omnicell, Inc. | Cranberry Township, PA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omnicell, Inc. | Milpitas, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pedigo Products, Inc. | Vancouver, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pryor Products | Oceanside, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Harloff Company, Inc. | Colorado Springs, CO, United States | 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.