Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K153690 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PriMatrix; Dermal Repair Scaffold; Rx Only; Sizes 0.2x26.5 cm (3 pack), 10x12cm, 10x25 cm, 20x25 cm,... | 2 | 09/30/2024 |
FEI # 3004170064 TEI Biosciences, Inc. |
| PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18m... | 2 | 09/30/2024 |
FEI # 3004170064 TEI Biosciences, Inc. |
| PriMatrix Meshed; Dermal Repair Scaffold; Rx Only; Sizes 20x25 cm (1:1), 3x3 cm (2:1), 4x4 cm (2:1),... | 2 | 09/30/2024 |
FEI # 3004170064 TEI Biosciences, Inc. |
| PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis. The device is supp... | 2 | 01/17/2018 |
FEI # 3004170064 TEI Biosciences |
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