VASCULAR SOLUTIONS LLC
Registration 2134812FEI 3002827704Maple Grove, MN
Owner/operator: Vascular Solutions LLC
- Develop Specifications But Do Not Manufacture At This Facility
- Manufacture Medical Device
- Manufacture Medical Device for Another Party (Contract Manufacturer)
- Repack or Relabel Medical Device
Renewal due by December 31, 2026
Registered through 2026. Renew between October 1 and December 31, 2026, to stay registered for 2027.
90days left in the window
The 2026 window
- Oct 1Window opens91 days left
- Nov 3Where you stand58 days left
- Dec 1Our pay-by date30 days left
- Dec 15Two weeks left16 days left
- Dec 23Holiday week8 days left
- Dec 29Two days left2 days left
- Dec 31Window closes0 days left
- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 75
- Added, last 12 months
- 1
FDA sets who pays the fee and who may qualify for a waiver; its fee page says so. The fee is paid only on FDA’s own fee site. Never through us. FDA’s fee page
The steps, in order
Pay FDA's annual feeYou
Order and pay the FY2027 establishment fee on FDA's Device Facility User Fee site. FDA emails you a PIN when you order.
FDA: registration and listing payment processWait for the payment confirmation numberYou
FDA emails a Payment Confirmation Number (PCN) once the payment processes, which FDA says typically takes several days. That is why we suggest paying by December 1.
FDA: registration and listing payment processRenew the registration in FDA's systemYou
Sign in to FDA's Unified Registration and Listing System (FURLS), complete the annual registration and apply your PIN and PCN. FDA does not count the registration as complete until both are applied.
FDA: device registration and listingReview every listingYou
In the same window, review each listing on file and report any changes, deletions and new listings. Your Listing Review Sheet puts every listing on one page.
FDA: device registration and listing
Every listed device 75
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| LMF | Agent, Absorbable Hemostatic, Collagen BasedGeneral, Plastic Surgery | Class 3 | 21 CFR 878.4490 | — |
| MGB | MANTA Vascular Closure DeviceDevice, Hemostasis, Vascular | Class 3 | — | P180025 |
| MGB | Device, Hemostasis, VascularUnknown | Class 3 | — | P990037 |
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary BypassCardiovascular | Class 2 | 21 CFR 870.4290 | K122301 |
| CAZ | Anesthesia Conduction KitAnesthesiology | Class 2 | 21 CFR 868.5140 | — |
| CAZ | TheraCath® Epidural Catheterization KitAnesthesia Conduction Kit | Class 2 | 21 CFR 868.5140 | — |
| CAZ | FlexBlock® Continuous Peripheral Nerve Block KitAnesthesia Conduction Kit | Class 2 | 21 CFR 868.5140 | — |
| CAZ | StimuCath® Continuous Peripheral Nerve Block KitAnesthesia Conduction Kit | Class 2 | 21 CFR 868.5140 | — |
| QEZ | Aspiration Thrombectomy CatheterCardiovascular | Class 2 | 21 CFR 870.5150 | K070403 |
| QEZ | Pronto V4 Extraction CatheterAspiration Thrombectomy Catheter | Class 2 | 21 CFR 870.5150 | K103405 |
| QEZ | Aspiration Thrombectomy CatheterCardiovascular | Class 2 | 21 CFR 870.5150 | K083784 |
| FCG | Biopsy NeedleGastroenterology, Urology | Class 2 | 21 CFR 876.1075 | K142377 |
and 63 more on your full dossier
What changed
- Dec 10, 2025Listing added: OFC — VSI Micro-Introducer Kit