FDA Device Intelligence
HomeORMCO CORPORATION › M.A.R.A.

M.A.R.A.

ORMCO CORPORATION · Model 600-3000 · UDI-DI 00889989074666

KMY Prescription
10
510(k) clearances
1,679
Adverse events
0
Recalls
112
Facilities

Description

M.A.R.A. KIT Mandibular Anterior Repositioning Appliance

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.