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SOMNOBRUX SPLINTS

Page Type
Cleared 510(K)
510(k) Number
K102909
510(k) Type
Traditional
Applicant
Somnomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2011
Days to Decision
438 days
Submission Type
Summary

SOMNOBRUX SPLINTS

Page Type
Cleared 510(K)
510(k) Number
K102909
510(k) Type
Traditional
Applicant
Somnomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2011
Days to Decision
438 days
Submission Type
Summary