Company ยท IL
DreaMed Diabetes, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 8, 2026 | K260062 | MODI System DreaMed Diabetes, Ltd., IL | QRX |
| Oct 3, 2023 | K232722 | endo.digital Platform DreaMed Diabetes, Ltd., IL | QCC |
| Sep 28, 2021 | K210561 | Advisor Pro Platform DreaMed Diabetes, Ltd., IL | QCC |
| Aug 28, 2020 | K201476 | DreaMed Advisor Pro DreaMed Diabetes, Ltd., IL | QCC |
| Jul 18, 2019 | K191370 | DreaMed Advisor Pro DreaMed Diabetes, Ltd., IL | QCC |
| Jun 12, 2018 | DEN170043 | DreaMed Advisor Pro DreaMed Diabetes, Ltd., IL | QCC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||