FDA Device Intelligence
HomeTrimed, INC. › Tools - FPS

Tools - FPS

Trimed, INC. · Model BNDROD-S · UDI-DI 00842188111112

HXP Prescription
5
510(k) clearances
160
Adverse events
1
Recalls
158
Facilities

Description

Bending Rod, 2.0mm/ 2.3mm

Recalls

DateFirmReason
2013-06-22Synthes USA HQ, Inc.A complaint was received of the tips of the Matrix 5.5.mm Left and Right Coronal Bender breaking while bending a spinal rod component of the Matrix System.

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.