# TIGHTLINE DEVELOPMENT

FEI: 3014150042
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: TightLine Development (#10056000)

Address: One Glenlake Parkway, Suite 650, Atlanta, GA, US



## Products

Total registered: 1
Top product codes: KDD
Regulation §: 878.4800

Proprietary names: eXodus

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014150042%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014150042