# KICO KNEE INNOVATION COMPANY

FEI: 3013552417
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Kico Knee Innovation Company (#10054916)

Address: Unit 1, 25 Frenchs Forest Rd E, Frenchs Forest New South Wales, 2086, AU

Mandatory US Agent: Encore Medical, L.P.

## Products

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

Proprietary names: KICo Probe

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013552417%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013552417