# SUREAX MEDICAL, CORPORATION

FEI: 3024682301
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Reprocess Single-Use Device
Owner/operator: SureAx Medical, Corporation (#10086251)

Address: 11107 Roselle St 237, San Diego, CA, US



## Products

Total registered: 1
Top product codes: DQX
Regulation §: 870.1330

Proprietary names: SureAx Guide

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223024682301%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3024682301