Home › Aesculap AG › ERGOPLANT
ERGOPLANT
Aesculap AG · Model DX254R · UDI-DI 04046963506360
EMM
Prescription
4
510(k) clearances
2
Adverse events
1
Recalls
132
Facilities
Description
BUSER ERGOPLANT Bone File, 7 1/2" (190 mm), double ended, width: 3 mm, 5 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-04-16 | Biomet Microfixation, Inc. | The working tips of the Stella Osteotomes are thicker than specification. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.