Data / Medical devices / United States / Fedex Supply Chain, Inc.
Fedex Supply Chain, Inc.: FDA-registered device maker in Olive Branch, MS, United States, 1 510(k) clearance
Fedex Supply Chain, Inc. is registered with the FDA (registration 3014197758) in Olive Branch, MS, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 2, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014197758
- Address
- 6750 Legacy Blvd, Suite 101, Olive Branch, MS, United States, 38654
- Owner or operator
- FedEx Supply Chain, Inc. (10056474)
- Roles
- Repackager or relabeler
- First device listed
- June 17, 2025
- Registered through
- 2026
- Brand names listed
- twiist system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alternate Controller Enabled Insulin Infusion Pump | QFG | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 2, 2025 | K250930 | twiist system | QFG | Substantially Equivalent | Deka Research & Development Corp. | accessdata.fda.gov |
Compare with other makers
Updated April 2, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.