Data / Medical devices / Tube, Tracheal (W/Wo Connector) / United States
FDA-registered makers of Tube, Tracheal (W/Wo Connector) in the United States: 39 establishments
39 establishments in the United States are registered with the FDA to make Tube, Tracheal (W/Wo Connector) (product code BTR). 20 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Tube, Tracheal (W/Wo Connector)
- Product code
- BTR
- Country
- United States
Makers of Tube, Tracheal (W/Wo Connector) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 30 | April 29, 2025 | 0 | 14 | 4 | api.fda.gov |
| Covidien | Lafayette, CO, United States | Specification developer | 14 | October 6, 2025 | 0 | 1 | 0 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 9 | January 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 7 | August 13, 2008 | 0 | 0 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Specification developer | 3 | May 11, 2012 | 0 | 0 | 0 | api.fda.gov |
| Boston Medical Products, Inc. | Shrewsbury, MA, United States | Manufacturer | 3 | February 12, 1993 | 0 | 0 | 0 | api.fda.gov |
| Salter Labs | El Paso, TX, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 3 | January 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| Bryan Medical Inc. | Cincinnati, OH, United States | Specification developer | 1 | November 25, 2020 | 0 | 0 | 0 | api.fda.gov |
| Clarus Medical, LLC. | Minneapolis, MN, United States | Manufacturer, Specification developer | 1 | April 28, 2009 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 1 | April 23, 2018 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Spencer, IN, United States | Manufacturer | 1 | April 23, 2018 | 0 | 0 | 0 | api.fda.gov |
| E. Benson Hood Laboratories, Inc. | Pembroke, MA, United States | Manufacturer | 1 | March 9, 1987 | 0 | 0 | 0 | api.fda.gov |
| Ecomed Solutions, LLC | Lindenhurst, IL, United States | Complaint file establishment, Specification developer | 1 | January 17, 2018 | 0 | 0 | 0 | api.fda.gov |
| Invotec International, Inc. | Jacksonville, FL, United States | Manufacturer | 1 | March 19, 1993 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Xomed, Inc. | Jacksonville, FL, United States | Manufacturer | 1 | April 15, 1993 | 0 | 0 | 0 | api.fda.gov |
| MedSource Labs, LLC | Chanhassen, MN, United States | Complaint file establishment, Specification developer | 1 | October 27, 2008 | 0 | 0 | 0 | api.fda.gov |
| NeVap Inc Inventory Management | San Jose, CA, United States | Specification developer | 1 | February 16, 2018 | 0 | 0 | 0 | api.fda.gov |
| Pipeline Medical Products, LLC | Weymouth, MA, United States | Specification developer | 1 | August 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Spiro Robotics Inc. | Hayward, CA, United States | Complaint file establishment, Specification developer | 1 | June 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Utah Medical Products, Inc. | Midvale, UT, United States | Manufacturer | 1 | March 16, 1993 | 0 | 0 | 0 | api.fda.gov |
| ARCH Medical Solutions - Memphis | Bartlett, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ARCH Medical Solutions - Memphis | Lexington, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ARCH Medical Solutions - Seabrook | Seabrook, NH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Armm, Inc. | Huntington Beach, CA, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BD Medical Development | Crown Point, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bound Tree Medical, LLC | Grand Prairie, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Command Medical Products, LLC. | Ormond Beach, FL, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Canton, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Exxelia Micropen | Honeoye Falls, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ferry Machine Corporation | Oakland, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ferry Machine Corporation | Little Ferry, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Globus Medical, Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Insert Molding Solutions, Inc. | Cumming, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | Spartanburg, SC, United States | Contract sterilizer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mackay Manufacturing, Inc. | Spokane Valley, WA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| N8 Medical LLC | Dublin, OH, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neurovision Medical Products, Inc. | Ventura, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nuvasive, Inc. | San Diego, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quadrant Technologies, LLC | Grayslake, IL, 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.