FDA Device Establishments · JSON-LD · Markdown

Kyocera Medical Technologies, Inc.

FEI 3007932279 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3007932279
Owner / OperatorKyocera Medical Technologies, Inc. (#10030880)
Address1289 Bryn Mawr Ave Ste A, Redlands, CA, US
Registration expiry2026
Initial importer flagY
Registered products2
Product codes (top 20)HWC, HTN
Regulation § (21 CFR)888.3040, 888.3030
Proprietary namesRenovis Cannulated Screw System

External sources

Source: openFDA. Public-domain (CC0).