Endoplus, Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| ENDOPLUS; Precision Laparoscopic Instruments; REF 346VA; Description 5mm Atraumatic Graspe recall (Z-2264-2013) | Endoplus, Inc. | 2013-09-21 |
| ENDOPLUS; Precision Laparoscopic Instruments; REF 345VA; Description 5 mm Traumatic Graspe recall (Z-2265-2013) | Endoplus, Inc. | 2013-09-21 |
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Every clearance here is in the API, with alerts when new ones post.