Medical Device Manufacturer · US , Lakewood , CO

Ceramed Corp. - FDA 510(k) Cleared Devices

16 submissions · 15 cleared · Since 1989

16

Total

15

Cleared

0

Denied

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

13 devices

1-13 of 13

Cleared Aug 20, 1996

PERMARIDGE SYRINGE

Cleared Aug 01, 1996

OSTEOGRAF STAINLESS STEEL SYRING

Cleared Apr 22, 1996

OSTEOGRAF/N-300 HYDROXYLAPATITE

Cleared Apr 18, 1996

OSTEOGRAF/LD-300 HYDROXYLAPATITE

Cleared Apr 18, 1996

OSTEOGRAFT/N-700 HYDROXYLAPTITE

Cleared Apr 15, 1996

PERMAMESH-D HYDROXYLAPATITE MATRIX

Cleared Jan 02, 1996

OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE

Cleared Oct 05, 1994

OSTEOGRAF/D-100 HYDROXYLAPATITE

Cleared Aug 23, 1994

OSTEOGRAF/LD-300 HYDROXYLAPATITE

Cleared Aug 21, 1992

PERMAMESH HYDROXYLAPATITE MATRIX

Cleared Jun 25, 1992

OSTEOGRAF/N-700 NATURAL HYDROXYLAPATITE 18-40 MESH

Cleared Dec 11, 1990

OSTEOGRAF/N NATURAL HYDROXYLAPATITE, 40-60 MESH

Cleared Sep 01, 1989

OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60