Medical Device Manufacturer · US , Mchenry , IL

Pentron Corp. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1984

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pentron Corp. Dental ✕

15 devices

1-12 of 15

Cleared Aug 01, 2002

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL

Cleared Feb 11, 1988

DUAL-CURE RADIOPAQUE

Cleared Jan 19, 1988

OPTEC SUPPLEMENTARY KIT

Cleared Jan 12, 1988

OPTEC STAIN CHARACTERIZATION AND MODIFICATION KIT

Cleared Nov 16, 1987

CODE #23 R SYSTEM (DENTIN ADHESIVE MATERIAL)

Cleared Oct 27, 1987

Cleared Nov 24, 1986

PENTRON HIGH STRENGTH PORCELAIN

Cleared Mar 04, 1986

CHAMELEON BONDING KIT

Cleared Dec 03, 1984

C-22 PIT & FISSURE SEALANT

Cleared May 22, 1984

Cleared May 22, 1984

Cleared May 22, 1984

NUMBER 21 R/R SYSTEM