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Ceramed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K962838PERMARIDGE SYRINGEAugust 20, 1996
K962786OSTEOGRAF STAINLESS STEEL SYRINGAugust 1, 1996
K960348OSTEOGRAF/N-300 HYDROXYLAPATITEApril 22, 1996
K960353OSTEOGRAF/LD-300 HYDROXYLAPATITEApril 18, 1996
K960368OSTEOGRAFT/N-700 HYDROXYLAPTITEApril 18, 1996
K960361PERMAMESH-D HYDROXYLAPATITE MATRIXApril 15, 1996
K960354PERMAMESH-D HYDROXYLAPATITE MATRIXMarch 20, 1996
K960362PERMAMESH HYDROXYLAPATITE MATRIXMarch 20, 1996
K960349PERMARIDGE HYDROXYLAPATITE MATRIXMarch 13, 1996
K954631OSTEOGRAF/N-BLOCCK HYDROXYLAPATITEJanuary 2, 1996
K942946OSTEOGRAF/D-100 HYDROXYLAPATITEOctober 5, 1994
K942212OSTEOGRAF/LD-300 HYDROXYLAPATITEAugust 23, 1994
K921468PERMAMESH HYDROXYLAPATITE MATRIXAugust 21, 1992
K921469OSTEOGRAF/N-700 NATURAL HYDROXYLAPATITE 18-40 MESHJune 25, 1992
K902295OSTEOGRAF/N NATURAL HYDROXYLAPATITE, 40-60 MESHDecember 11, 1990
K891173OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60September 1, 1989