Medical Device Recalls
-
1 result found
510(K) Number: K181112 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model prepar... | 2 | 12/06/2021 | Orchestrate Orthodontic Technologies, Inc. |
-