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Myoaligner Appliance

Page Type
Cleared 510(K)
510(k) Number
K230548
510(k) Type
Traditional
Applicant
Myohealth Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2024
Days to Decision
339 days
Submission Type
Summary

Myoaligner Appliance

Page Type
Cleared 510(K)
510(k) Number
K230548
510(k) Type
Traditional
Applicant
Myohealth Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2024
Days to Decision
339 days
Submission Type
Summary