Data / Medical devices / Binder, Elastic / United States
FDA-registered makers of Binder, Elastic in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Binder, Elastic (product code KMO). 0 have a 510(k) clearance or PMA approval on file and 0 have 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
- Binder, Elastic
- Product code
- KMO
- Country
- United States
Makers of Binder, Elastic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alpha Medical L.L.C. | Rock Hill, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Core Products International Inc | Chetek, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| D3D,LLC | Sioux Falls, SD, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Elastic Therapy, LLC | Asheboro, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frank Stubbs | Oxnard, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HK Surgical, Inc. | San Clemente, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lenjoy Medical Engineering, Inc. | Gardena, CA, United States | 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 | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, 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 | |
| Optp LLC | Minneapolis, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SIGVARIS Inc. - Holland Facility | Holland, MI, 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.