FDA applicant
Intravent Medical Partners, LP
FDA records 2 decisions for Intravent Medical Partners, LP (Hershey, PA) from 2021 to 2025: 2 510(k) clearances. All are in product code HAW (Neurological Stereotaxic Instrument). Its devices cite 3 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Intravent Medical Partners”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Intravent Medical Partners, LP’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Intravent Medical Partners, LP’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report