# HARBOR MEDTECH, INC.

FEI: 3010097129
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Harbor MedTech, Inc. (#10090866)

Address: 21076 Bake Parkway, Suite 100, Lake Forest, CA, US



## Products

Total registered: 1
Top product codes: KGN
Regulation §: —


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010097129%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010097129