FDA Device Intelligence
Home › ORMCO CORPORATION › Nexus Clear Roth

Nexus Clear Roth

ORMCO CORPORATION · Model 437-3110 · UDI-DI 00889989046571

NJM Prescription
10
510(k) clearances
23
Adverse events
1
Recalls
47
Facilities

Description

U1R .022 +12/+5/0

Recalls

DateFirmReason
2013-11-19Ultradent Products, Inc.Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic Brackets because the design control process was not complete prior to distribution.

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.