# Implant Technology, Inc.

- Location (FDA's records): Secaucus, NJ
- FDA decisions: 13 (1983–1995): 13 510(k) clearances
- Product codes: JDI (6), BTO (3), MEH (1), LPH (1), LZV (1), KXA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K921525: Hip Joint Metal/Polymer Semi-Constrained Prothesis (Jan 11, 1995)
- K915617: LSF HA Coated Femoral Hip (May 28, 1992)
- K920021: LSF Total Hip System - Muller-Type Acetabular Cup (Mar 25, 1992)
- K913616: LSF Diagnostic Related Group Cemented Hip (Nov 7, 1991)
- K902727: LSF Cemented Femoral Hip (Aug 9, 1990)
- K901460: LSF (TM) Total Hip System (May 22, 1990)
- K891472: Implant Technology Bone Cement Extractor (May 2, 1989)
- K884432: Modified LSF Total Hip System (Dec 9, 1988)

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