# Canady Biotechnology LLC

FEI: 3008849319
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: US Medical Innovations (#10047595)

Address: 6930 Carroll Ave, Takoma Park, MD, US



## Products

Total registered: 2
Top product codes: GEI, OAB
Regulation §: 878.4400

Proprietary names: Canady Helios Cold Plasma XL-1000CP Ablation System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008849319%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008849319