ImpediMed Limited
ImpediMed Limited holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 1 FDA device recall on record.
Top product codes for ImpediMed Limited
FDA recalls by ImpediMed Limited
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by ImpediMed Limited
- K260224 — MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)
- K253224 — MySOZO Software version 6.0.1.2 (SW version 6.0.1.2)
- K232089 — SOZO Pro
- K230530 — SOZO Pro
- K230531 — SOZO Pro
- K203473 — SOZO
- K193410 — SOZO Body Fluid Analyzer
- K190529 — SOZO
- K180126 — SOZO
- K172507 — SOZO
- K172122 — SOZO
- K130338 — IMPEDIMED - BIS EXTRA CELLULAR FLUID ANALYSIS
- K100811 — IMPEDIMED - EXTRACELLULAR FLUID ANALYZER MODEL: L-DEX U400
Data sourced from openFDA. This site is unofficial and independent of the FDA.