Richard Wolf GmbH
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression recall (Z-1753-2025) | Richard Wolf GmbH | 2025-05-13 |
| FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051 recall (Z-1422-2023) | Richard Wolf GmbH | 2023-04-24 |
| FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051 recall (Z-1423-2023) | Richard Wolf GmbH | 2023-04-24 |
| FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685 recall (Z-1424-2023) | Richard Wolf GmbH | 2023-04-24 |
| FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685 recall (Z-1425-2023) | Richard Wolf GmbH | 2023-04-24 |
| Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) combination syst recall (Z-2706-2020) | Richard Wolf GmbH | 2020-07-27 |
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Every clearance here is in the API, with alerts when new ones post.