Contract manufacturerFlextronics International USA (Buffalo Grove, IL)IllinoisClinical chemistryClass II
Flextronics International USA
Contract manufacturer ยท Buffalo Grove, IL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3011536730 (openFDA record; or search FDA's registration database)
- FEI number
- 3011536730
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer for export only; Contract manufacturer
- Owner or operator
- Flextronics International USA, Inc. (FDA owner/operator no. 9006592)
- Registered address
- 700 Corporate Grove Drive, Buffalo Grove, IL 60089
- Contract listings
- 5 device listings, 5 product codes, first listed Jun 16, 2020
- 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 |
|---|---|---|---|---|---|
| NBW | System, Test, Blood Glucose, Over The Counter | Class II | Clinical chemistry | Contract manufacturing | Jun 16, 2020 |
| QBJ | Integrated Continuous Glucose Monitoring System, Factory Calibrated | Class II | Clinical chemistry | Contract manufacturing | Sep 19, 2023 |
| QLG | Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems | Class II | Clinical chemistry | Contract manufacturing | Jun 16, 2020 |
| SAF | Integrated Continuous Glucose Monitor For Non-Intensive Glucose Monitoring, Over-The-Counter | Class II | Clinical chemistry | Contract manufacturing | Jun 12, 2024 |
| SBH | Integrated Continuous Glucose Monitor For Non-Intensive Glucose Management, Over-The-Counter | Class II | Clinical chemistry | Contract manufacturing | Jun 12, 2024 |