Data / Medical devices / Bag, Bile Collecting / United States
FDA-registered makers of Bag, Bile Collecting in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Bag, Bile Collecting (product code EXF). 3 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
- Bag, Bile Collecting
- Product code
- EXF
- Country
- United States
Makers of Bag, Bile Collecting in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Argon Medical Devices Inc. | Athens, TX, United States | Contract manufacturer, Manufacturer | 1 | January 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Bard Access Systems, Inc. | Salt Lake City, UT, United States | Specification developer | 1 | September 8, 1994 | 0 | 0 | 0 | api.fda.gov |
| Remington Medical, Inc. | Alpharetta, GA, United States | Manufacturer | 1 | August 12, 1999 | 0 | 3 | 0 | api.fda.gov |
| C.R. Bard, Inc. | Queensbury, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| C.R. Bard, Inc. | Covington, GA, United States | Contract sterilizer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marlen MFG. & Development Co. | Bedford, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merit Medical Systems, Inc. | South Jordan, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sterigenics U.S., LLC | Salt Lake City, UT, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Uresil, LLC | Skokie, IL, 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.