Contract manufacturerGLOBAL INTERCONNECT, INC. (Pocasset, MA)MassachusettsNeurologyOrthopedicGeneral and plastic surgeryClass II
GLOBAL INTERCONNECT, INC.
Contract manufacturer · Pocasset, MA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004920696 (openFDA record; or search FDA's registration database)
- FEI number
- 3004920696
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Global Interconnect, Inc. (FDA owner/operator no. 10050573)
- Registered address
- 11 JONATHAN BOURNE DR, Pocasset, MA 02559
- Contract listings
- 10 device listings, 5 product codes, first listed Dec 3, 2015
- 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 |
|---|---|---|---|---|---|
| GWJ | Stimulator, Auditory, Evoked Response | Class II | Neurology | Contract manufacturing | May 1, 2024 |
| GWM | Device, Monitoring, Intracranial Pressure | Class II | Neurology | Contract manufacturing | Dec 3, 2015 |
| GXY | Electrode, Cutaneous | Class II | Neurology | Contract manufacturing | Nov 16, 2018 |
| HRX | Arthroscope | Class II | Orthopedic | Contract manufacturing | Apr 2, 2025 |
| QAI | Powered Microneedle Device | Class II | General and plastic surgery | Contract manufacturing | Dec 12, 2024 |