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. General & Plastic Surgery ✕

3 devices

1-3 of 3

Cleared Mar 20, 1996

PERMAMESH-D HYDROXYLAPATITE MATRIX

General & Plastic Surgery · 55d

Cleared Mar 20, 1996

PERMAMESH HYDROXYLAPATITE MATRIX

General & Plastic Surgery · 55d

Cleared Mar 13, 1996

PERMARIDGE HYDROXYLAPATITE MATRIX

General & Plastic Surgery · 48d