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EndoRing®
US ENDODONTICS, LLC · Model 00818365021390 · UDI-DI 00818365028481
EIL
Prescription
8
510(k) clearances
10
Adverse events
0
Recalls
143
Facilities
Description
EndoRing® II Kit with REDUCED GLARE Metal Ruler and e-Foam® Rotary HD Inserts EndoRing® Silver Rotary HD e-foam® Insert Refill Pack
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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.