# Osteoimplant Technology, Inc.

- Location (FDA's records): Hunt Valley, MD
- FDA decisions: 21 (1996–2005): 21 510(k) clearances
- Product codes: LPH (7), JDI (6), LZO (2), LWJ (1), JDK (1), HSD (1), HSH (1), HRY (1), KWZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 11 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Imaging Therapeutics, Inc.: 1 (https://510kreport.com/company/imaging-therapeutics)

## Its most-cited devices
- K022779: Oti Unicondular Interpositional Spacer (2002), cited by 1

## Recent decisions
- K040685: Z - Series Modular Total Hip System Plasma Coated (Jan 25, 2005)
- K041443: Oti Alumina Ceramic Femoral Head System (Nov 16, 2004)
- K040225: Oti Alumina Ceramic Femoral Head System (May 6, 2004)
- K032729: Z-Series Modular Total Hip System (Dec 3, 2003)
- K030608: Oti Bone Cement Plug (Jun 12, 2003)
- K022779: Oti Unicondular Interpositional Spacer (Nov 20, 2002)
- K021822: R120 Modular Total Hip System (Jul 23, 2002)
- K012762: MJS Posterior Stabilized Knee System (Dec 11, 2001)

Source page: https://510kreport.com/company/osteoimplant-technology