FDA Device Intelligence
Home › Gc America Inc. › COE®

COE®

Gc America Inc. · Model 260211 · UDI-DI 10386040000734

EBH Prescription
10
510(k) clearances
8
Adverse events
0
Recalls
192
Facilities

Description

COE® Regular-Perforated, Individual Tray, #21 Lower

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.