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Trylon Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033033VIZILITE-BLUE ORAL EXAM KITNovember 22, 2004
K011488SPIRABRUSH CX BIOPSY INSTRUMENTFebruary 22, 2002
K012070ORALLITE COMPREHENSIVE EXAM TRAYNovember 27, 2001
K003995SPECULITE/ORALLITEMarch 16, 2001
K963391SPECULITEDecember 12, 1997
K955790PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAYMarch 21, 1996
K953364SPECULITEDecember 8, 1995