Contract manufacturerJunoPacific, Inc. (Brooklyn Park, MN)MinnesotaNeurologyCardiovascularOphthalmicClass IIIClass II
JunoPacific, Inc.
Contract manufacturer ยท Brooklyn Park, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2134604 (openFDA record; or search FDA's registration database)
- FEI number
- 3002623849
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- JUNOPACIFIC INC. (FDA owner/operator no. 9036368)
- Registered address
- 8701 95th Avenue North, Brooklyn Park, MN 55445
- Contract listings
- 5 device listings, 4 product codes, first listed Feb 22, 2021
- 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 |
|---|---|---|---|---|---|
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief | Class III | Neurology | Contract manufacturing | Nov 21, 2022 |
| MXC | Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection) | Class II | Cardiovascular | Contract manufacturing | Feb 22, 2021 |
| NVY | Permanent Defibrillator Electrodes | Class III | Cardiovascular | Contract manufacturing | Nov 21, 2022 |
| OOE | Ophthalmic Femtosecond Laser | Class II | Ophthalmic | Contract manufacturing | Jul 31, 2023 |