Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032104 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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PROKERA, non-sterile - Product Usage: Biologic corneal bandage. | 2 | 12/09/2020 | TissueTech, Inc. |
PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage. | 2 | 12/09/2020 | TissueTech, Inc. |
PROKERA Plus, non-sterile - Product Usage: Biologic corneal bandage. | 2 | 12/09/2020 | TissueTech, Inc. |
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