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Pentron Laboratory Technologies

FDA Regulatory Profile

Pentron Laboratory Technologies appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 17, 2003.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023742SCULPTURE PLUS NANO-HYBRID COMPOSITEJanuary 17, 2003
K023499GOLD CORE PLUSJanuary 13, 2003
K023502JEWEL CAST PLUSDecember 18, 2002
K023501GOLD CORE 35December 18, 2002
K020555SONATA MICRO HYBRID COMPOSITEApril 22, 2002

FDA data resources