Dental Device Guide
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Not currently registered with FDA under this name

Ceramed Corp.

Lakewood, CO, United States. Named as applicant on 13 dental 510(k) clearances between 1989 and 1996. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
131989–1996
Markets registered in
1United States
Establishments
0—
1989: 11990: 11992: 21994: 21996: 719801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Ceramed Corp. as the applicant.

Decided510(k)DeviceDevice type
20 Aug 1996K962838PERMARIDGE SYRINGELYC Synthetic Bone Grafting Material
1 Aug 1996K962786OSTEOGRAF STAINLESS STEEL SYRINGLYC Synthetic Bone Grafting Material
22 Apr 1996K960348OSTEOGRAF/N-300 HYDROXYLAPATITELYC Synthetic Bone Grafting Material
18 Apr 1996K960368OSTEOGRAFT/N-700 HYDROXYLAPTITELYC Synthetic Bone Grafting Material
18 Apr 1996K960353OSTEOGRAF/LD-300 HYDROXYLAPATITELYC Synthetic Bone Grafting Material
15 Apr 1996K960361PERMAMESH-D HYDROXYLAPATITE MATRIXLYC Synthetic Bone Grafting Material
2 Jan 1996K954631OSTEOGRAF/N-BLOCCK HYDROXYLAPATITELYC Synthetic Bone Grafting Material
5 Oct 1994K942946OSTEOGRAF/D-100 HYDROXYLAPATITELYC Synthetic Bone Grafting Material
23 Aug 1994K942212OSTEOGRAF/LD-300 HYDROXYLAPATITELYC Synthetic Bone Grafting Material
21 Aug 1992K921468PERMAMESH HYDROXYLAPATITE MATRIXLYC Synthetic Bone Grafting Material
25 Jun 1992K921469OSTEOGRAF/N-700 NATURAL HYDROXYLAPATITE 18-40 MESHLYC Synthetic Bone Grafting Material
11 Dec 1990K902295OSTEOGRAF/N NATURAL HYDROXYLAPATITE, 40-60 MESHLYC Synthetic Bone Grafting Material
1 Sep 1989K891173OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60LYC Synthetic Bone Grafting Material

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.