Data / Medical devices / United States / VENTUREMED GROUP, Inc
VENTUREMED GROUP, Inc: FDA-registered device maker in Plymouth, MN, United States, 2 510(k) clearances
VENTUREMED GROUP, Inc is registered with the FDA (registration 3012696653) in Plymouth, MN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated September 11, 2020. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3012696653
- Address
- 2800 Campus Dr. Suite 50, Plymouth, MN, United States, 55441
- Owner or operator
- VentureMed Group, Inc. (10052004)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- May 31, 2016
- Registered through
- 2026
- Brand names listed
- FLEX Vessel Prep System, FLEX Vessel Prep System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous, Cutting/Scoring | PNO | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 11, 2020 | K202187 | FLEX Vessel Prep System | PNO | Substantially Equivalent | Venturemed Group, Inc. | accessdata.fda.gov |
| May 25, 2016 | K152789 | FLEX SCORING CATHETER | PNO | Substantially Equivalent | Venturemed Group | accessdata.fda.gov |
Compare with other makers
Updated September 11, 2020. 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.