Ceramed Corp.
Ceramed Corp. appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 20, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 16
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K962838 | PERMARIDGE SYRINGE | August 20, 1996 |
| K962786 | OSTEOGRAF STAINLESS STEEL SYRING | August 1, 1996 |
| K960348 | OSTEOGRAF/N-300 HYDROXYLAPATITE | April 22, 1996 |
| K960353 | OSTEOGRAF/LD-300 HYDROXYLAPATITE | April 18, 1996 |
| K960368 | OSTEOGRAFT/N-700 HYDROXYLAPTITE | April 18, 1996 |
| K960361 | PERMAMESH-D HYDROXYLAPATITE MATRIX | April 15, 1996 |
| K960354 | PERMAMESH-D HYDROXYLAPATITE MATRIX | March 20, 1996 |
| K960362 | PERMAMESH HYDROXYLAPATITE MATRIX | March 20, 1996 |
| K960349 | PERMARIDGE HYDROXYLAPATITE MATRIX | March 13, 1996 |
| K954631 | OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE | January 2, 1996 |
| K942946 | OSTEOGRAF/D-100 HYDROXYLAPATITE | October 5, 1994 |
| K942212 | OSTEOGRAF/LD-300 HYDROXYLAPATITE | August 23, 1994 |
| K921468 | PERMAMESH HYDROXYLAPATITE MATRIX | August 21, 1992 |
| K921469 | OSTEOGRAF/N-700 NATURAL HYDROXYLAPATITE 18-40 MESH | June 25, 1992 |
| K902295 | OSTEOGRAF/N NATURAL HYDROXYLAPATITE, 40-60 MESH | December 11, 1990 |
| K891173 | OSTEOGRAF/P PERIODONTAL HYDROXYLAPATITE, 40-60 | September 1, 1989 |