Medical Device Recalls
-
1 result found
510(K) Number: K220287 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 Invisalign System ... | 2 | 01/26/2023 | Align Technology Inc |
-