FDA Device Intelligence
Homedevemed GmbH › Reicodent

Reicodent

devemed GmbH · Model 02-SU 1-2 C · UDI-DI 04061644036622

EMR Prescription
1
510(k) clearances
105
Adverse events
0
Recalls
58
Facilities

Description

Periodontal file # 1S-2S "Sugarman"; Mesial / Distal 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.