Medical Device Manufacturer · US , Mchenry , IL

Pentron Corp. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1984

Total

Cleared

Denied

Pentron Corp. has 15 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1984 to 2002.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Pentron Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pentron Corp.

15 devices

1-15 of 15

Cleared Aug 01, 2002

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL

OPTEC SUPPLEMENTARY KIT

K874275 · EBF

Dental · 91d

Cleared Jan 12, 1988

OPTEC STAIN CHARACTERIZATION AND MODIFICATION KIT

K874162 · EBF

Dental · 91d

Cleared Nov 16, 1987

CODE #23 R SYSTEM (DENTIN ADHESIVE MATERIAL)

PENTRON HIGH STRENGTH PORCELAIN

K864404 · EIH

Dental · 14d

Cleared Mar 04, 1986

CHAMELEON BONDING KIT

K854803 · EBF

Dental · 92d

Cleared Dec 03, 1984

C-22 PIT & FISSURE SEALANT

Pentron Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Pentron Corp.

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