Data / Medical devices / Enteral Syringes With Enteral Specific Connectors / United States
FDA-registered makers of Enteral Syringes With Enteral Specific Connectors in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Enteral Syringes With Enteral Specific Connectors (product code PNR). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Enteral Syringes With Enteral Specific Connectors
- Product code
- PNR
- Country
- United States
Makers of Enteral Syringes With Enteral Specific Connectors in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 4 | April 30, 2019 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 3 | December 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Norfolk, NE, United States | Manufacturer | 2 | December 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Deland, FL, United States | Manufacturer | 2 | December 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medela LLC | Mchenry, IL, United States | Manufacturer, Specification developer | 2 | February 15, 2017 | 0 | 0 | 0 | api.fda.gov |
| American Health Packaging | Columbus, OH, United States | Complaint file establishment, Reprocessor | 1 | August 6, 2019 | 0 | 0 | 0 | api.fda.gov |
| Intl. Medical Industries | Pompano Beach, FL, United States | Manufacturer | 1 | October 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| CLAYENS Crystal Lake, LLC | Crystal Lake, 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.