Data / Medical devices / Binder, Medical, Therapeutic / United States
FDA-registered makers of Binder, Medical, Therapeutic in the United States: 26 establishments
26 establishments in the United States are registered with the FDA to make Binder, Medical, Therapeutic (product code MDR). 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
- Binder, Medical, Therapeutic
- Product code
- MDR
- Country
- United States
Makers of Binder, Medical, Therapeutic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aci Medical, LLC | San Marcos, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alta Medical LLC | Milwaukee, WI, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| American Breast Care LP | Marietta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blue Lagoon Inc. Dba Tec-Ops | Hickory, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BSN medical Inc. | Charlotte, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BSN medical inc. | Hickory, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ben Guard healthcare Inc | Cincinnati, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Discovery Direct, Inc. | Easton, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Encompass Group, LLC. | McDonough, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gus Gear, Inc. | Pittsburgh, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Julius Zorn, Inc. | Cuyahoga Falls, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| L&R Usa Inc. | Milwaukee, WI, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laacke & Joys Company LLC | Brookfield, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medi MFG., Inc. | Whitsett, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medi Usa, LP | Whitsett, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| My True Image MFG. | Richmond, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nester Hosiery, LLC | Mount Airy, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pattersonpouch | Roanoke, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pure Medical Inc. | Wauwatosa, WI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SIGVARIS Inc. - Holland Facility | Holland, MI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tarry Medical Products, Inc. | Danbury, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Hygenic Company, LLC | Akron, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Marena Group, LLC. | Lawrenceville, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thuasne, LLC | Hamlet, NC, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vitaform, Inc. | Dana Point, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wear Ease Inc. | Boise, ID, 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.