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INUMI™ Flex Needle

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233884
510(k) Type
Traditional
Applicant
Galvanize Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
166 days
Submission Type
Summary

INUMI™ Flex Needle

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233884
510(k) Type
Traditional
Applicant
Galvanize Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
166 days
Submission Type
Summary