Data / Medical devices / Circuit, Breathing (W Connector, Adaptor, Y Piece) / United States
FDA-registered makers of Circuit, Breathing (W Connector, Adaptor, Y Piece) in the United States: 35 establishments
35 establishments in the United States are registered with the FDA to make Circuit, Breathing (W Connector, Adaptor, Y Piece) (product code CAI). 6 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.
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- Device
- Circuit, Breathing (W Connector, Adaptor, Y Piece)
- Product code
- CAI
- Country
- United States
Makers of Circuit, Breathing (W Connector, Adaptor, Y Piece) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 1 | October 26, 1981 | 0 | 0 | 0 | api.fda.gov |
| Anesthesia Associates, Inc. | San Marcos, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 1 | December 27, 1983 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Lafayette, CO, United States | Specification developer | 1 | January 3, 1986 | 0 | 0 | 0 | api.fda.gov |
| King Systems Corporation. | Noblesville, IN, United States | Manufacturer, Repackager or relabeler, Specification developer | 1 | March 9, 1988 | 0 | 2 | 1 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Specification developer | 1 | July 23, 1993 | 0 | 0 | 0 | api.fda.gov |
| Westmed, Inc. | Tucson, AZ, United States | Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 1 | April 24, 1991 | 0 | 0 | 0 | api.fda.gov |
| All Quality & Services, Inc. | Garland, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B & B Medical Technologies, Inc. | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bio-Med Devices, Inc. | Guilford, CT, United States | 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 | |
| Covidien | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Customed, Inc. | Fajardo, PR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien LLC | Mansfield, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | Powell, TN, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | New Tazewell, TN, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Datex-Ohmeda, Inc. | Madison, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genesis Medical Plastics Ltd. Co. | Cypress, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Instrumentation Industries, Incorporated | Bethel Park, PA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Invent Medical Corporation | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intersurgical Inc. | Indianapolis, IN, United States | Contract manufacturer, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medi-Part,inc. | Harvey, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Laredo | Laredo, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 27 | 5 | api.fda.gov | |
| Medline Industries, LP - SPT | Waukegan, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medron, LLC | Salt Lake City, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mercury Medical Enterprises, LLC | Clearwater, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Fluidics Division Parker Hannifin Corp. | Hatfield, PA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safeguard Us Operating, LLC | Huntersville, NC, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smooth-Bor Plastics | Laguna Hills, CA, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SharpMed, LLC | Scottsdale, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 2 | 1 | api.fda.gov | |
| Telesair, Inc. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.