Ventris Medical

Ventris Medical holds 5 FDA 510(k) medical device clearances, first cleared 2022, most recent 2026.

Top product codes for Ventris Medical

MQV — Orthopedic4 devices
KGN — Unknown1 device

Recent clearances by Ventris Medical

K260596 — Collagen Wound PowderCode KGN·2026-07-02
K250556 — Porous Biologic ScaffoldCode MQV·2025-03-21
K240765 — Porous Biologic ScaffoldCode MQV·2024-12-18
K240458 — Synthetic Bone PuttyCode MQV·2024-03-07
K221644 — Synthetic Bone PuttyCode MQV·2022-09-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.