Contract manufacturerVirtex (Anoka, MN)MinnesotaGastroenterology and urologyGeneral hospitalClass IIUnclassified
Virtex
Contract manufacturer · Anoka, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2183673 (openFDA record; or search FDA's registration database)
- FEI number
- 2183673
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Virtex (FDA owner/operator no. 2183673)
- Registered address
- 6700 Bunker Lake Blvd. NW, Anoka, MN 55303
- Contract listings
- 3 device listings, 3 product codes, first listed Mar 28, 2008
- 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 |
|---|---|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | Class II | Gastroenterology and urology | Contract manufacturing | Mar 28, 2008 |
| LIL | Monitor, Penile Tumescence | Unclassified | Gastroenterology and urology | Contract manufacturing | Dec 18, 2020 |
| LZH | Pump, Infusion, Enteral | Class II | General hospital | Contract manufacturing | Apr 2, 2008 |