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Unisplint Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K830675
ORAL SPONGE
March 24, 1983
K820944
DENTAL ARCH BAR
May 5, 1982