Omnilife Science Inc.
5 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Offset Femoral Alignment Guide, 2mm x 6; Product Code: KS 67022 Product Usage: The instrum recall (Z-2454-2015) | Omnilife Science Inc. | 2015-08-24 |
| Offset Femoral Alignment Guide 4mm x 6; Product Code: KS 67024 Product Usage: The instrume recall (Z-2455-2015) | Omnilife Science Inc. | 2015-08-24 |
| APEX INTERFACE Hemi 54X and Flared 56X, 3 Hole Acetabular Shells; Model: H5-12354, H5-1135 recall (Z-2445-2015) | Omnilife Science Inc. | 2015-08-21 |
| Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex AR recall (Z-2064-2015) | Omnilife Science Inc. | 2015-07-14 |
| Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA recall (Z-2241-2014) | Omnilife Science Inc. | 2014-08-15 |
Track Omnilife Science Inc. automatically
Every clearance here is in the API, with alerts when new ones post.