Last synced on 25 January 2026 at 3:41 am

Tesera-k PL System and Tesera-k XL System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242771
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
188 days
Submission Type
Summary

Tesera-k PL System and Tesera-k XL System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242771
510(k) Type
Traditional
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
188 days
Submission Type
Summary