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SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221306
510(k) Type
Traditional
Applicant
Gyrus Acmi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
267 days
Submission Type
Summary

SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221306
510(k) Type
Traditional
Applicant
Gyrus Acmi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
267 days
Submission Type
Summary