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Reicodent

devemed GmbH · Model 02-54 · UDI-DI 04061644040780

EMJ Prescription
6
510(k) clearances
638
Adverse events
0
Recalls
236
Facilities

Description

Root elevator 4.5 mm H-Type A

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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.