Data / Medical devices / Media, Electroconductive / United States
FDA-registered makers of Media, Electroconductive in the United States: 18 establishments
18 establishments in the United States are registered with the FDA to make Media, Electroconductive (product code GYB). 8 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Media, Electroconductive
- Product code
- GYB
- Country
- United States
Makers of Media, Electroconductive in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Parker Laboratories, Inc. | Fairfield, NJ, United States | Manufacturer | 3 | August 9, 1985 | 0 | 2 | 0 | api.fda.gov |
| BSG Corp | Acton, MA, United States | Manufacturer | 1 | May 14, 1997 | 0 | 0 | 0 | api.fda.gov |
| Carol Cole Company dba NuFACE | Vista, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | December 30, 2016 | 0 | 0 | 0 | api.fda.gov |
| D. O. Weaver And Company | Aurora, CO, United States | Manufacturer | 1 | September 28, 1988 | 0 | 0 | 0 | api.fda.gov |
| Electro-Cap Intl., Inc. | Eaton, OH, United States | Manufacturer | 1 | January 5, 2012 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | June 29, 2000 | 0 | 0 | 0 | api.fda.gov |
| Nse Products, Inc. | Provo, UT, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | September 13, 2002 | 0 | 0 | 0 | api.fda.gov |
| Prizm Medical, Inc. | Buford, GA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 1 | July 30, 2004 | 0 | 0 | 0 | api.fda.gov |
| Amrex-Zetron, Inc. | Paramount, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Krenerb, LLC | Hockessin, DE, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NORTHWEST COSMETIC LABS, LLC d/b/a Elevation Labs Idaho | Idaho Falls, ID, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Silgan Unicep Packaging, LLC. | Sandpoint, ID, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum Us LLC | Eagan, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Silgan Unicep Packaging, LLC. | Spokane, WA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum US LLC | San Antonio, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum US LLC | Brookings, SD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wasatch Product Development, LLC | Draper, UT, United States | Contract 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.