FDA Device Intelligence
Home › MIZUHO ORTHOPEDIC SYSTEMS, INC. › SPLINT, BUCK'S TRAC, CONVOLUTED, SIZE XS

SPLINT, BUCK'S TRAC, CONVOLUTED, SIZE XS

MIZUHO ORTHOPEDIC SYSTEMS, INC. · Model 371XS · UDI-DI 00842430114366

HSP
1
510(k) clearances
6
Adverse events
1
Recalls
65
Facilities

Recalls

DateFirmReason
2024-02-27Emergency Products & ResearchFailure of adhesive to secure the pole insert.

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.