Medical Device Recalls
-
|
1 result found
510(K) Number: K243278 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438; | 2 | 03/24/2026 |
FEI # 1000121052 Straumann USA LLC |
-







