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Reicodent

devemed GmbH · Model 02-2500-13 C · UDI-DI 04061644037360

EKD Prescription
2
510(k) clearances
26
Adverse events
0
Recalls
73
Facilities

Description

Periotome 2.0 mm, angled sidewards COMFORT | SL | single ended

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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.