Data / Medical devices / Screen, Leaded, Operator Radiation Protector / United States
FDA-registered makers of Screen, Leaded, Operator Radiation Protector in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Screen, Leaded, Operator Radiation Protector (product code EAK). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Screen, Leaded, Operator Radiation Protector
- Product code
- EAK
- Country
- United States
Makers of Screen, Leaded, Operator Radiation Protector in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aadco Medical, Inc. | Randolph, VT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alimed, LLC | Dedham, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Burlington Medical, LLC | Newport News, VA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Del Medical, Inc. | Bloomingdale, IL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ecls | Saint Louis, MO, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Egg Medical, Inc. | Roseville, MN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| FT Industries, Inc | Bessemer, AL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Image Diagnostics, Inc. | Fitchburg, MA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Infab, LLC. | Camarillo, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phillips Safety Products, Inc. | Middlesex, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RAMPART IC, Inc | Birmingham, AL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RAMPART IC, Inc | Vestavia, AL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Salus Scientific Corp | Charleston, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Techno-Aide, Inc. | Whites Creek, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| trans radial solutions | Roebuck, SC, 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.