FDA Device Intelligence
Home › KLS-Martin L.P. › IPS

IPS

KLS-Martin L.P. · Model 60-011-23-09-LP · UDI-DI 00888118148780

ELE Prescription
4
510(k) clearances
3
Adverse events
0
Recalls
3
Facilities

Description

IMPLANT, 1 QUADRANT, REMOVABLE MUA, W/OUT FINAL, LP, TI-6AL-4V

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.