FDA Device Intelligence
Home › PEDICRAFT, INC. › Pedi Board

Pedi Board

PEDICRAFT, INC. · Model 02523 · UDI-DI 00766923025239

NOD
0
510(k) clearances
3
Adverse events
0
Recalls
40
Facilities

Description

Pedi Board 2x4

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.