FDA Device Intelligence
HomeEXTREMITY MEDICAL, LLC › KinematX

KinematX

EXTREMITY MEDICAL, LLC · Model 137-30001-S · UDI-DI 00842078112014

JWJ Prescription
1
510(k) clearances
497
Adverse events
0
Recalls
38
Facilities

Description

Radial Body Assembly - LEFT, +0

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.