Data / Medical devices / Apparatus, Autotransfusion / United States
FDA-registered makers of Apparatus, Autotransfusion in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Apparatus, Autotransfusion (product code CAC). 14 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 2, 2026.
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- Device
- Apparatus, Autotransfusion
- Product code
- CAC
- Country
- United States
Makers of Apparatus, Autotransfusion in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 9 | October 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 9 | October 23, 2014 | 0 | 1 | 0 | api.fda.gov |
| Haemonetics Corporation | Boston, MA, United States | Specification developer | 6 | November 15, 2022 | 0 | 10 | 0 | api.fda.gov |
| Medtronic Perfusion Systems | Minneapolis, MN, United States | Specification developer | 5 | August 22, 2018 | 0 | 1 | 0 | api.fda.gov |
| Haemonetics Corporation | Salt Lake City, UT, United States | Manufacturer | 2 | December 3, 2010 | 0 | 0 | 0 | api.fda.gov |
| Inari Medical, Inc. | Irvine, CA, United States | Manufacturer | 2 | July 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| LivaNova USA, INC. | Arvada, CO, United States | Manufacturer | 2 | September 9, 1999 | 0 | 2 | 0 | api.fda.gov |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 2 | May 2, 1983 | 0 | 0 | 0 | api.fda.gov |
| 3T Medical Systems Inc. | Edison, NJ, United States | Specification developer | 1 | December 16, 1997 | 0 | 0 | 0 | api.fda.gov |
| Atrium Medical Corporation | Merrimack, NH, United States | Manufacturer | 1 | September 3, 2021 | 0 | 7 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Specification developer | 1 | October 24, 2008 | 0 | 0 | 0 | api.fda.gov |
| Globus Medical, Inc. | Audubon, PA, United States | Manufacturer | 1 | April 2, 1999 | 0 | 0 | 0 | api.fda.gov |
| Inquis Medical, Inc. | Menlo Park, CA, United States | Manufacturer | 1 | May 14, 2024 | 0 | 0 | 0 | api.fda.gov |
| Procell Surgical Inc. | Canton, MA, United States | Complaint file establishment, Specification developer | 1 | June 1, 2020 | 0 | 0 | 0 | api.fda.gov |
| Isomedix Operations Inc. | San Diego, CA, United States | Contract sterilizer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Multisource Manufacturing LLC | Longmont, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Miller Technical Services | Plymouth, MI, 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.