FDA Device Intelligence
HomeLIMACORPORATE SPA › Smart SPACE SHOULDER

Smart SPACE SHOULDER

LIMACORPORATE SPA · Model 0023.R4.N33 · UDI-DI 08033390239509

QHEKWSMBF Prescription
1
510(k) clearances
8
Adverse events
2
Recalls
35
Facilities

Description

Smart SPACE SHOULDER - Glenoid 3D Positioner-RIGHT4-NOT STER

Recalls

DateFirmReason
2026-03-12Linkbio Corp.The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
2021-06-25Tornier S.A.S.Potential patient exposure to the graphite substrate.

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.