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XCELLARISPRO TWIST microneedling device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241790
510(k) Type
Traditional
Applicant
Dermaroller GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
258 days
Submission Type
Summary

XCELLARISPRO TWIST microneedling device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241790
510(k) Type
Traditional
Applicant
Dermaroller GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
258 days
Submission Type
Summary