# Kalitec Direct LLC DBA Kalitec Medical

FEI: 3009165919
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Kalitec Medical (#10037099)

Address: 1819 Main St Ste 303, Sarasota, FL, US



## Products

Total registered: 1
Top product codes: NKB
Regulation §: 888.3070

Proprietary names: NIDO Pedicle Screw System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009165919%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009165919