Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K213812 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PALACOS MV pro 40; PALACOS MV pro 80. Model/Catalog Number: 5150633; 5150635. Radiopaque, poly(m... | 2 | 09/25/2026 |
FEI # 3006406161 Heraeus Medical GmbH (Dental Division) |
| Brand Name: PALACOS Product Name: PALACOS MV pro 40; PALACOS MV pro 80 Model/Catalog Number: 51506... | 2 | 01/14/2026 |
FEI # 3006406161 Heraeus Medical GmbH (Dental Division) |
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