FDA Device Intelligence
Home › ORTHOPEDIATRICS CORP. › PediFlex

PediFlex

ORTHOPEDIATRICS CORP. · Model 01-1001-0004 · UDI-DI 00840194493741

HXG Prescription
1
510(k) clearances
160
Adverse events (7 deaths)
0
Recalls
234
Facilities

Description

Flat Tamp, Large

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.