FDA Device Intelligence
Home › ORMCO CORPORATION › Ormco

Ormco

ORMCO CORPORATION · Model 673-3672 · UDI-DI 00889989059205

ECM Prescription
2
510(k) clearances
4
Adverse events
0
Recalls
86
Facilities

Description

LING TUBE HZ W/LOCK-HKS 036X072 UL/LR

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.