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devemed

devemed GmbH · Model 753-15 F · UDI-DI 04061644032044

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

Description

dev-lux 2.5 mm | Periolux Area: mesial F-LINE | RS | angulated, blue-coded

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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.