Data / Medical devices / United States / GEODIS Logistics
GEODIS Logistics: FDA-registered device maker in Clayton, IN, United States, 2 510(k) clearances
GEODIS Logistics is registered with the FDA (registration 3016267994) in Clayton, IN, United States. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 21, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3016267994
- FEI number
- 2000004234
- Address
- 1716 Innovation Blvd., Clayton, IN, United States, 46118
- Owner or operator
- GEODIS Logistics (10022608)
- Roles
- Repackager or relabeler
- First device listed
- April 19, 2022
- Registered through
- 2027
- Brand names listed
- Boudreaux's, Compound W, Efferdent, Little Remedies, Nix, Rid
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Absorbent Tipped, Non-Sterile | KXF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Applicator, Ent | KCJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cleaner, Denture, Mechanical | JER | 1 | Repackager or relabeler | accessdata.fda.gov |
| Detectors And Removers, Lice, (Including Combs) | LJL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Unit, Cryosurgical, Accessories | GEH | 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 |
|---|---|---|---|---|---|---|
| March 21, 2017 | K163401 | Nix Ultra Lice Treatment Kit | LJL | Substantially Equivalent | Medtech Products, Inc. | accessdata.fda.gov |
| September 15, 2016 | K161294 | Compound W Wart Removal System Dual Power | GEH | Substantially Equivalent | Medtech Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Detectors And Removers, Lice, (Including Combs)
- All makers of Unit, Cryosurgical, Accessories
- All makers of Applicator, Absorbent Tipped, Non-Sterile
- All makers of Applicator, Ent
- All makers of Syringe, Irrigating (Non Dental)
- All makers of Cleaner, Denture, Mechanical
Updated March 21, 2017. 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.