Data / Medical devices / Temporary, Internal Use Hemostatic / United States
FDA-registered makers of Temporary, Internal Use Hemostatic in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Temporary, Internal Use Hemostatic (product code POD). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Temporary, Internal Use Hemostatic
- Product code
- POD
- Country
- United States
Makers of Temporary, Internal Use Hemostatic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 3 | March 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Z-Medica, LLC | North Haven, CT, United States | Manufacturer, Repackager or relabeler | 3 | March 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Z-Medica, LLC | Wallingford, CT, United States | Manufacturer, Repackager or relabeler | 3 | March 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Advamedica Inc. | Cambridge, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | January 5, 2023 | 0 | 0 | 0 | api.fda.gov |
| Beeken Biomedical LLC | Newton, MA, United States | Complaint file establishment, Specification developer | 1 | September 25, 2019 | 0 | 1 | 0 | api.fda.gov |
| Benefit Coatings, Inc. | Stratford, CT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carwild Corp. | New London, CT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Robling Medical, LLC | Youngsville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weslacova | North Wilkesboro, NC, United States | Contract 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.