Amendia, Inc
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| 01.4mm x 457mm (18in) K-Wire, Threaded Blunt, Ref 9080B-18T, Qty: 1 per pack, Material: SS recall (Z-1885-2017) | Amendia, Inc | 2017-04-25 |
| Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical inter recall (Z-0966-2017) | Amendia, Inc | 2017-01-09 |
| Black Widow Plate 19mm Plate, Part Number TBP119; Black Widow Plate 23mm Plate, Part Numbe recall (Z-0886-2017) | Amendia, Inc | 2016-12-22 |
| Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part N recall (Z-0887-2017) | Amendia, Inc | 2016-12-22 |
| Optimus Fixed Awl recall (Z-0891-2017) | Amendia, Inc | 2016-12-22 |
| Zeus-P Lumbar Interbody Device recall (Z-0827-2017) | Amendia, Inc | 2016-12-20 |
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Every clearance here is in the API, with alerts when new ones post.