FDA Device Intelligence
Home › DEPUY (IRELAND) › ACTIS

ACTIS

DEPUY (IRELAND) · Model 3010-01-060 · UDI-DI 10603295548652

QBO
2
510(k) clearances
105
Adverse events
0
Recalls
15
Facilities

Description

ACTIS HIP SYSTEM BROACH SIZE 6

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.