# Kyocera Medical Technologies, Inc.

FEI: 3007932279
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198
Owner/operator: Kyocera Medical Technologies, Inc. (#10030880)

Address: 1289 Bryn Mawr Ave Ste A, Redlands, CA, US



## Products

Total registered: 2
Top product codes: HWC, HTN
Regulation §: 888.3040, 888.3030

Proprietary names: Renovis Cannulated Screw System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007932279%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007932279