# POINTIMPLANT Co., Ltd

FEI: 3011891801
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: PointImplant Co Ltd (#10083213)

Address: B1 and 3F, 7, Hyoyeol-ro, Buk-gu, Busan, 46509, KR

Mandatory US Agent: Mtech Group LLC

## Products

Total registered: 1
Top product codes: DZA
Regulation §: 872.4130

Proprietary names: Final Drill, Point Drill, Cortical Drill, Lance Drill, Bone Profile Drill, Tissue Punch Drill, Fixture Tap Drill, SideCut Drill, Initial Drill

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011891801%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011891801