# RESELUTE

FEI: 3042025564
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Reselute (#10094154)

Address: 701 W Main Street, Ste 420, Durham, NC, US



## Products

Total registered: 1
Top product codes: LXH
Regulation §: 888.4540

Proprietary names: Reselute Tibial Intramedullary Instrument Tray

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223042025564%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3042025564