# GEODIS

FEI: 3008087383
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: GEODIS (#10030802)

Address: 450 Lillard Drive, Sparks, NV, US



## Products

Total registered: 2
Top product codes: LRC, PGW
Regulation §: 874.4420, 882.4560

Proprietary names: SPINPLUS 3-GUIDE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008087383%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008087383