FDA Device Intelligence
HomeLM-Dental › LMDental

LMDental

LM-Dental · Model 25ESGREYTU · UDI-DI 06438311001272

EJB
8
510(k) clearances
39
Adverse events
1
Recalls
267
Facilities

Description

Mirror handle 25 ES grey DTS U, Diagnostics

Recalls

DateFirmReason
2008-05-09Biomet 3i, Inc.The drill malfunctions while in use. The drill has been observed to become lodged in the handle.

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.