# CLARIPI INC.

FEI: 3015537315
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Reprocess Single-Use Device; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: CLARIPI Inc. (#10060777)

Address: 11 Ihwajang 1-gil, Jongro-gu, Seoul, 03100, KR

Mandatory US Agent: ClariPi USA Inc.

## Products

Total registered: 1
Top product codes: LLZ
Regulation §: 892.2050

Proprietary names: ClariCT.AI

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015537315%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015537315
