DreaMed Diabetes, Ltd.

DreaMed Diabetes, Ltd. holds 6 FDA 510(k) medical device clearances, first cleared 2018, most recent 2026.

Top product codes for DreaMed Diabetes, Ltd.

QCC — Clinical Chemistry5 devices
QRX — Clinical Chemistry1 device

Recent clearances by DreaMed Diabetes, Ltd.

K260062 — MODI SystemCode QRX·2026-09-08
K232722 — endo.digital PlatformCode QCC·2023-10-03
K210561 — Advisor Pro PlatformCode QCC·2021-09-28
K201476 — DreaMed Advisor ProCode QCC·2020-08-28
K191370 — DreaMed Advisor ProCode QCC·2019-07-18
DEN170043 — DreaMed Advisor ProCode QCC·2018-06-12

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