Data / Medical devices / United States / Intravent Medical Partners LP
Intravent Medical Partners LP: FDA-registered device maker in Blue Bell, PA, United States, 1 510(k) clearance
Intravent Medical Partners LP is registered with the FDA (registration 3021591288) in Blue Bell, PA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 5, 2025. 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
- 3021591288
- Address
- 1730 Walton Rd Ste 110, Blue Bell, PA, United States, 19422
- Owner or operator
- inTRAvent Medical Partners LP (10084271)
- Roles
- Specification developer
- First device listed
- December 6, 2025
- Registered through
- 2026
- Brand names listed
- SOLOPASS 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Neurological Stereotaxic Instrument | HAW | 2 | Specification developer | accessdata.fda.gov |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | 2 | 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 5, 2025 | K251317 | SOLOPASS 2.0 System | HAW | Substantially Equivalent | Intravent Medical Partners | accessdata.fda.gov |
Compare with other makers
- All makers of System, Imaging, Pulsed Doppler, Ultrasonic
- All makers of Neurological Stereotaxic Instrument
Updated September 5, 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.