# FIRST USE LLC

FEI: 3005370013
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: FIRST USE LLC (#9077490)

Address: 2500 SANDERSVILLE RD., LEXINGTON, KY, US



## Products

Total registered: 1
Top product codes: HRH
Regulation §: 886.4350

Proprietary names: GAYHEART CORNEAL TREPHINE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005370013%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005370013