Contract manufacturerNELIPAK PHOENIX (Phoenix, AZ)ArizonaGeneral and plastic surgeryClass II
NELIPAK PHOENIX
Contract manufacturer ยท Phoenix, AZ
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3012137049 (openFDA record; or search FDA's registration database)
- FEI number
- 3012137049
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Nelipak Phoenix (FDA owner/operator no. 10055012)
- Registered address
- 3720 West Washington Street, Phoenix, AZ 85009
- Contract listings
- 1 device listings, 1 product codes, first listed Aug 22, 2017
- 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 |
|---|---|---|---|---|---|
| FTA | Light, Surgical, Accessories | Class II | General and plastic surgery | Contract manufacturing | Aug 22, 2017 |