Micro Therapeutics, Inc.
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300 recall (Z-2773-2026) | Micro Therapeutics, Inc. | 2026-07-22 |
| Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300 recall (Z-2774-2026) | Micro Therapeutics, Inc. | 2026-07-22 |
| Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-1 recall (Z-1245-2025) | Micro Therapeutics, Inc. | 2025-03-05 |
| Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-1 recall (Z-1246-2025) | Micro Therapeutics, Inc. | 2025-03-05 |
| The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole recall (Z-1252-2024) | Micro Therapeutics, Inc. | 2024-03-04 |
| The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole recall (Z-1253-2024) | Micro Therapeutics, Inc. | 2024-03-04 |
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Every clearance here is in the API, with alerts when new ones post.