FDA Device Intelligence
Home › ORTHOPEDIATRICS CORP. › ACL

ACL

ORTHOPEDIATRICS CORP. · Model 01-1008-2530 · UDI-DI 00841132124277

FZH Prescription
4
510(k) clearances
12
Adverse events
0
Recalls
4
Facilities

Description

2.5MM X 300MM GUIDE WIRE, SMOOTH, COCR

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.