Last synced on 25 January 2026 at 3:41 am

LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100610
510(k) Type
Traditional
Applicant
Lutronic Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2011
Days to Decision
323 days
Submission Type
Summary

LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100610
510(k) Type
Traditional
Applicant
Lutronic Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2011
Days to Decision
323 days
Submission Type
Summary