Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K231963 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Pr... | 2 | 10/05/2023 |
FEI # 3016090213 Blue Belt Technologies, Inc |
| CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S | 2 | 01/11/2024 |
FEI # 3016090213 Blue Belt Technologies, Inc |
-







