Contract manufacturerVAULT PARAGON GROUP, INC. (Garden City, ID)IdahoGeneral hospitalClass II
VAULT PARAGON GROUP, INC.
Contract manufacturer · Garden City, ID
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3018681450 (openFDA record; or search FDA's registration database)
- FEI number
- 3018681450
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Specification developer; Contract manufacturer
- Owner or operator
- VAULT PARAGON GROUP INC (FDA owner/operator no. 10081504)
- Registered address
- 199 E 52nd Street, Ste. 150, Garden City, ID 83714
- Contract listings
- 1 device listings, 4 product codes, first listed Jan 30, 2026
- 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 |
|---|---|---|---|---|---|
| FMF | Syringe, Piston | Class II | General hospital | Contract manufacturing | Jan 30, 2026 |
| FMI | Needle, Hypodermic, Single Lumen | Class II | General hospital | Contract manufacturing | Jan 30, 2026 |
| MEG | Syringe, Antistick | Class II | General hospital | Contract manufacturing | Jan 30, 2026 |
| ONB | Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System | Class II | General hospital | Contract manufacturing | Jan 30, 2026 |