FDA Device Intelligence
Home › ALLESEE AOA-PRO › Transpalatal Arch

Transpalatal Arch

ALLESEE AOA-PRO · Model 3000-0033 · UDI-DI 00889989038590

KMY Prescription
10
510(k) clearances
1,702
Adverse events
0
Recalls
114
Facilities

Description

Transpalatal Arch

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.