# ULTRASPECT USA, LLC

FEI: 3018788582
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: UltraSPECT USA, LLC (#10081545)

Address: 101 Dillion Court, Gray, TN, US



## Products

Total registered: 2
Top product codes: LLZ, KPS
Regulation §: 892.2050, 892.1200

Proprietary names: Xpress3.Cardiac including ASCS, Xpress.Cardiac including ACSC

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223018788582%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3018788582