Contract manufacturerTD SYNNEX (Groveport, OH)OhioAnesthesiologyCardiovascularClass II
TD SYNNEX
Contract manufacturer ยท Groveport, OH
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3026740087 (openFDA record; or search FDA's registration database)
- FEI number
- 3026740087
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- TD SYNNEX (FDA owner/operator no. 10087381)
- Registered address
- 5300 Centerpoint Pkwy, Groveport, OH 43125
- Contract listings
- 5 device listings, 3 product codes, first listed Mar 10, 2023
- 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 |
|---|---|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | Class II | Anesthesiology | Contract manufacturing | Mar 10, 2023 |
| DQA | Oximeter | Class II | Cardiovascular | Contract manufacturing | Mar 6, 2024 |
| DQK | Computer, Diagnostic, Programmable | Class II | Cardiovascular | Contract manufacturing | Jan 2, 2024 |