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PROPEL device

Page Type
Cleared 510(K)
510(k) Number
K150392
510(k) Type
Traditional
Applicant
PROPEL ORTHODONTICS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
212 days
Submission Type
Summary

PROPEL device

Page Type
Cleared 510(K)
510(k) Number
K150392
510(k) Type
Traditional
Applicant
PROPEL ORTHODONTICS LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2015
Days to Decision
212 days
Submission Type
Summary