GEODIS Logistics

FDA Device Registration & Listing · Clayton, IN, US · Registration 3016267994

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016267994
FEI Number
2000004234
Entity Name
GEODIS Logistics
City/State/Country
Clayton, IN, US
Establishment Address
1716 Innovation Blvd., Clayton, IN 46118, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
GEODIS Logistics (Owner Number: 10022608)
Owner / Operator Contact Address
7101 Executive Center Drive,, Suite 333, Brentwood, TN 37027, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K161294
PMA Number
N/A

All Registered Proprietary Names

Boudreaux's Compound W

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2023-03-01
GEH Unit, Cryosurgical, Accessories General, Plastic Surgery Class 2 878.4350 2022-04-19

Official Correspondent

Brad Elrod

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GEODIS Logistics
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3022238661 GEODIS Logistics Northampton, PA, US
2000004234 Geodis Logistics Clayton, IN, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190651 Erbe Elektromedizin GmbH ERBECRYO 2 Cryosurgical Unit; ERBECRYO 2 1-pedal footswitch, Extension cable f. ERBECRYO 2 footswitch; Flexible Cryoprobe; ERBECRYO 2 Cart, VIO-Cart, Wire basket; Connecting hoses, switching valves, adapter 2020-01-07
K760953 Spembly Medical , Ltd. DEEP FREEZE SYSTEM (DFS-30) 1976-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016267994. Last updated year: 2026. Please use registration number 3016267994 when referencing this establishment in official correspondence.
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