Data / Medical devices / Catheter, Peritoneal, Long-Term Indwelling / United States
FDA-registered makers of Catheter, Peritoneal, Long-Term Indwelling in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Catheter, Peritoneal, Long-Term Indwelling (product code FJS). 5 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
- Catheter, Peritoneal, Long-Term Indwelling
- Product code
- FJS
- Country
- United States
Makers of Catheter, Peritoneal, Long-Term Indwelling in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Covidien LLC | Mansfield, MA, United States | Specification developer | 11 | January 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Mozarc Medical Us LLC | Mansfield, MA, United States | Specification developer | 11 | January 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Merit Medical Systems, Inc. | South Jordan, UT, United States | Manufacturer | 7 | May 21, 2012 | 0 | 3 | 0 | api.fda.gov |
| Medical Components Inc | Harleysville, PA, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | September 5, 2012 | 0 | 0 | 0 | api.fda.gov |
| PFM Medical, Inc | Carlsbad, CA, United States | Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler | 1 | March 13, 2012 | 0 | 1 | 0 | api.fda.gov |
| Martech Medical Products | Harleysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merit Medical Systems, Inc. | Houston, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Point Medical Corp. | Crown Point, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paragon Medical - Mansfield, Bridgemedica | Mansfield, MA, 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.