Home › devemed GmbH › Reicodent

Reicodent

devemed GmbH · Model 02-720-24 · UDI-DI 04061644043095

EMJ Prescription

510(k) clearances

641

Adverse events

Recalls

241

Facilities

Description

Root elevator "Seldin" # 4R H-Type A

Query this across every FDA database — by API.

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

Get your free API key Read the docs

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.