FDA Device Intelligence
Home › devemed GmbH › Reicodent

Reicodent

devemed GmbH · Model 02-2010-29-31 · UDI-DI 04061644047772

EIY Prescription
5
510(k) clearances
18
Adverse events
0
Recalls
189
Facilities

Description

Filling Instrument "White" # 29,31 Burnisher Octagonal handle, solid, serrated

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 keyRead 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.