FDA Device Intelligence
Home › ORMCO CORPORATION › Ormco

Ormco

ORMCO CORPORATION · Model 866-4019 · UDI-DI 00889989068306

JEX Prescription
7
510(k) clearances
89
Adverse events
0
Recalls
235
Facilities

Description

DAMON CLEAR DEBONDING PLIER

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.