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/ DreaMed Diabetes, Ltd.
DreaMed Diabetes, Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K232722
endo.digital Platform
October 3, 2023
K210561
Advisor Pro Platform
September 28, 2021
K201476
DreaMed Advisor Pro
August 28, 2020
K191370
DreaMed Advisor Pro
July 18, 2019
DEN170043
DreaMed Advisor Pro
June 12, 2018