FDA applicant
Dyne Medical Group, Inc.
FDA records 2 decisions for Dyne Medical Group, Inc. (Gyeonggi-Do, KR) from 2024 to 2026: 2 510(k) clearances. Most are in product codes FGB (Ureteroscope And Accessories, Flexible/Rigid) and ODC (Endoscope Channel Accessory). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Dyne Medical Group, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Dyne Medical Group, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report