Data / Medical devices / Button, Nasal Septal / United States
FDA-registered makers of Button, Nasal Septal in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Button, Nasal Septal (product code LFB). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Button, Nasal Septal
- Product code
- LFB
- Country
- United States
Makers of Button, Nasal Septal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Boston Medical Products, Inc. | Shrewsbury, MA, United States | Manufacturer | 1 | July 3, 1997 | 0 | 0 | 0 | api.fda.gov |
| E. Benson Hood Laboratories, Inc. | Pembroke, MA, United States | Manufacturer | 1 | May 15, 1992 | 0 | 0 | 0 | api.fda.gov |
| Freudenberg Medical, LLC | Carpinteria, CA, United States | Manufacturer | 1 | September 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Medical Innovations International | Rochester, MN, United States | Complaint file establishment, Manufacturer | 1 | November 28, 2001 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Xomed, Inc. | Jacksonville, FL, United States | Manufacturer | 1 | October 17, 1978 | 0 | 0 | 0 | api.fda.gov |
| Summit Medical LLC | Saint Paul, MN, United States | Manufacturer | 1 | November 24, 1998 | 0 | 1 | 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.