Data / Medical devices / United States / Phraxis Inc
Phraxis Inc: FDA-registered device maker in Minneapolis, MN, United States, 1 PMA approval
Phraxis Inc is registered with the FDA (registration 3014146191) in Minneapolis, MN, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated May 15, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014146191
- Address
- 333 Hennepin Ave E, Unit 1903, Minneapolis, MN, United States, 55414
- Owner or operator
- Phraxis Inc (10093541)
- Roles
- Specification developer
- First device listed
- May 31, 2025
- Registered through
- 2026
- Brand names listed
- EndoForce Connector for Endovascular Venous Anastomosis
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Covered Stent Vascular Connector, Hemodialysis Access Circuit | SEQ | 3 | Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| May 15, 2025 | P240004 | EndoForce Connector for Endovascular Venous Anastomosis | SEQ | 2 | July 18, 2025 | accessdata.fda.gov |
Updated July 18, 2025. 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.