Contract manufacturerVANGUARD-EMS (Beaverton, OR)OregonCardiovascularClass IIClass III
VANGUARD-EMS
Contract manufacturer · Beaverton, OR
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004363082 (openFDA record; or search FDA's registration database)
- FEI number
- 3004363082
- Registered for
- FDA registration year 2027
- Establishment types
- Contract manufacturer
- Owner or operator
- Vanguard EMS, Inc. (FDA owner/operator no. 9059001)
- Registered address
- 3725 SW Hocken Ave, Beaverton, OR 97005
- Contract listings
- 6 device listings, 2 product codes, first listed Dec 1, 2016
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| PPN | Percutaneous Catheter, Ultrasound | Class II | Cardiovascular | Contract manufacturing | Dec 1, 2016 |
| QMG | Shockwave Intravascular Lithotripsy System | Class III | Cardiovascular | Contract manufacturing | Mar 3, 2021 |