# Ceramed Corp.

- Location (FDA's records): Lakewood, CO
- FDA decisions: 17 (1989–1999): 16 510(k) clearances and 1 original PMA approval
- Product codes: LYC (13), LZK (2), FWP (1), NPZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dentsply Interntional: 4 (https://510kreport.com/company/dentsply-interntional)
- Dentsply International, Inc.: 3 (https://510kreport.com/company/dentsply-international)
- Dio Department Dsi, Inc.: 1 (https://510kreport.com/company/dio-department-dsi)
- Bioform, Inc.: 1 (https://510kreport.com/company/bioform)

## Its most-cited devices
- K921468: Permamesh Hydroxylapatite Matrix (1992), cited by 2
- K942212: Osteograf/LD-300 Hydroxylapatite (1994), cited by 1
- K921469: Osteograf/N-700 Natural Hydroxylapatite 18-40 Mesh (1992), cited by 1
- K902295: Osteograf/N Natural Hydroxylapatite, 40-60 Mesh (1990), cited by 1
- K960353: Osteograf/LD-300 Hydroxylapatite (1996), cited by 1
- K960368: Osteograft/N-700 Hydroxylaptite (1996), cited by 1

## Recent decisions
- P990033: Pepgen P-15 (Oct 25, 1999)
- K962838: Permaridge Syringe (Aug 20, 1996)
- K962786: Osteograf Stainless Steel Syring (Aug 1, 1996)
- K960348: Osteograf/N-300 Hydroxylapatite (Apr 22, 1996)
- K960353: Osteograf/LD-300 Hydroxylapatite (Apr 18, 1996)
- K960368: Osteograft/N-700 Hydroxylaptite (Apr 18, 1996)
- K960361: Permamesh-D Hydroxylapatite Matrix (Apr 15, 1996)
- K960354: Permamesh-D Hydroxylapatite Matrix (Mar 20, 1996)

Source page: https://510kreport.com/company/ceramed