FDA Device Intelligence
Home › FUSION ORTHOPEDICS, LLC › LSI Arthroereisis Peg

LSI Arthroereisis Peg

FUSION ORTHOPEDICS, LLC · Model TN-LD-9003 · UDI-DI 00819034029488

MJW Prescription
1
510(k) clearances
7
Adverse events (1 deaths)
0
Recalls
5
Facilities

Description

(not in use)

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.