# Corflex Caribe

FEI: 3010621943
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Repack or Relabel Medical Device; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Corflex Global, LLC (#1218997)

Address: Zona Franca Industrial de San Isidro, antigua nave MFI-2, Santo Domingo Este, 15801, DO

Mandatory US Agent: Corflex

## Products

Total registered: 1
Top product codes: ITQ
Regulation §: 890.3475

Proprietary names: CKI STRAP 12", CKI / WHEATON STRAP 8", CKI/ WHEATON STRAP 12", CKI / WHEATON STRAP 10", CKI STRAP 10"

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010621943%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010621943