Last synced on 18 April 2025 at 11:05 pm

FLEXIROOT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852305
510(k) Type
Traditional
Applicant
FACIAL ALVEODENTAL IMPLANT REHABILITATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1985
Days to Decision
140 days

FLEXIROOT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852305
510(k) Type
Traditional
Applicant
FACIAL ALVEODENTAL IMPLANT REHABILITATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1985
Days to Decision
140 days