Landos, Inc.
Landos, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1997.
Top product codes for Landos, Inc.
Recent clearances by Landos, Inc.
- K964226 — MEMORY STAPLE (20 SIZES AVAILABLE)
- K971068 — 34MM SCARF THREAD-HEAD(TM) SCREW
- K971069 — TWIST-OFF (TM) SCREW
- K971070 — SCARF THREAD-HEAD (TM) HEAD SCREW
- K961732 — KAR
- K970846 — 22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD
- K953111 — CORAIL
- K962233 — TWIST-OFF SCREW
- K962236 — SCARF THREAD-HEAD SCREW
- K960642 — NANCY NAIL
- K943727 — BIOSTOP G BONE CEMENT RESTRICTOR
- K933108 — TITAN TROCHANTERO-DIAHYSEAL TOTAL HIP PROSTHESIS
- K935185 — MORPHOMETRIC TOTAL HIP PROSTHESIS
- K932935 — TITAN DYSPLASIC TOTAL HIP PROSTHESIS
- K933567 — EUROFORM TOTAL HIP PROSTHESIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.