Stryker Leibinger GmbH & Co. KG
5 FDA 510(k) clearances · Recalling firm
◉ Watch Stryker Leibinger GmbH & Co. KG
| Record | Firm | Date |
|---|---|---|
| 8000-021-002, Scopis ENT Software with TGS with Sofware Version: NOVA 3.6.0 RC16. Scopis i recall (Z-1885-2024) | Stryker Leibinger GmbH & Co. KG | 2024-05-23 |
| Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization recall (Z-1785-2024) | Stryker Leibinger GmbH & Co. KG | 2024-05-08 |
| Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis recall (Z-1234-2023) | Stryker Leibinger GmbH & Co. KG | 2023-03-08 |
| QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Fl recall (Z-1149-2017) | Stryker Leibinger GmbH & Co. KG | 2017-02-08 |
| 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silic recall (Z-1150-2017) | Stryker Leibinger GmbH & Co. KG | 2017-02-08 |
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Every clearance here is in the API, with alerts when new ones post.