Last synced on 14 November 2025 at 11:06 pm

NightGuard Flex

Page Type
Cleared 510(K)
510(k) Number
K212448
510(k) Type
Traditional
Applicant
SprintRay Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2021
Days to Decision
99 days
Submission Type
Summary

NightGuard Flex

Page Type
Cleared 510(K)
510(k) Number
K212448
510(k) Type
Traditional
Applicant
SprintRay Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2021
Days to Decision
99 days
Submission Type
Summary