FDA Device Intelligence
Home › MAKO SURGICAL CORP. › RESTORIS

RESTORIS

MAKO SURGICAL CORP. · Model 186040-03 · UDI-DI 00848486009892

OQHOQILPHMEHOQGJDILZO Prescription
1
510(k) clearances
8
Adverse events
0
Recalls
54
Facilities

Description

Femoral Head, CoCr, 12/14 Taper

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.