# InterX Technologies

FEI: 3004786509
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: InterX Technologies (#10051305)

Address: 3465 Technology Dr., Suite A, Plano, TX, US



## Products

Total registered: 1
Top product codes: GXY
Regulation §: 882.1320

Proprietary names: InterX Self-Adhesive Dual Electrode - Non-Sterile

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004786509%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004786509