Ceramed Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceramed Corp. - FDA 510(k) Cleared Devices
16
Total
15
Cleared
0
Denied
Ceramed Corp. has 15 FDA 510(k) cleared dental devices. Based in Lakewood, US.
Historical record: 15 cleared submissions from 1989 to 1996.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ceramed Corp.
16 devices
Cleared
Aug 20, 1996
PERMARIDGE SYRINGE
Dental
29d
Cleared
Aug 01, 1996
OSTEOGRAF STAINLESS STEEL SYRING
Dental
15d
Cleared
Apr 22, 1996
OSTEOGRAF/N-300 HYDROXYLAPATITE
Dental
88d
Cleared
Apr 18, 1996
OSTEOGRAF/LD-300 HYDROXYLAPATITE
Dental
84d
Cleared
Apr 18, 1996
OSTEOGRAFT/N-700 HYDROXYLAPTITE
Dental
84d
Cleared
Apr 15, 1996
PERMAMESH-D HYDROXYLAPATITE MATRIX
Dental
81d
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
Cleared
Jan 02, 1996
OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE
Dental
88d
Cleared
Oct 05, 1994
OSTEOGRAF/D-100 HYDROXYLAPATITE
Dental
104d
Cleared
Aug 23, 1994
OSTEOGRAF/LD-300 HYDROXYLAPATITE
Dental
109d
Cleared
Aug 21, 1992
PERMAMESH HYDROXYLAPATITE MATRIX
Dental
147d
Cleared
Jun 25, 1992
OSTEOGRAF/N-700 NATURAL HYDROXYLAPATITE 18-40 MESH
Dental
90d
Cleared
Dec 11, 1990
OSTEOGRAF/N NATURAL HYDROXYLAPATITE, 40-60 MESH
Dental
203d
Cleared
Sep 01, 1989
OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60
Dental
179d