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Reicodent

devemed GmbH · Model 02-968-4 · UDI-DI 04061644052196

EIG Prescription
8
510(k) clearances
34
Adverse events
0
Recalls
336
Facilities

Description

Retractor 55x11 mm | 215 mm "Obwegeser" bent upwards

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.