FDA Device Intelligence
Home › devemed GmbH › Reicodent

Reicodent

devemed GmbH · Model 02-3201-00 C · UDI-DI 04061644062829

EKT Prescription
0
510(k) clearances
3
Adverse events
0
Recalls
46
Facilities

Description

Spoon curette 4.0 mm | 3.0 mm COMFORT | SL | double ended

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.