FDA Device Intelligence
Home › Life Spine, Inc. › ARx SAI

ARx SAI

Life Spine, Inc. · Model 17-11540-19 · UDI-DI 00190837194758

OURNKB Prescription
1
510(k) clearances
1,406
Adverse events (5 deaths)
1
Recalls
154
Facilities

Recalls

DateFirmReason
2025-11-03Orthofix U.S. LLCLabeling contains claims that are not consistently present.

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.