# XTREEM PULSE

FEI: 3012470925
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: XTREEM PULSE (#10057865)

Address: 690 Washington St, # 4B, New York, NY, US



## Products

Total registered: 1
Top product codes: NFO
Regulation §: 882.5890

Proprietary names: PureLift Pro Plus

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012470925%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012470925