FDA Device Intelligence
HomeETABLISSEMENTS ANTHOGYR › Anthogyr OSTEOTOME

Anthogyr OSTEOTOME

ETABLISSEMENTS ANTHOGYR · Model EXO_FULLS · UDI-DI 03663394483377

EMM
4
510(k) clearances
2
Adverse events
1
Recalls
132
Facilities

Recalls

DateFirmReason
2008-04-16Biomet 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 docs
Data 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.