FDA Device Intelligence
Home › Stryker GmbH › REMOTION

REMOTION

Stryker GmbH · Model 300-4200 · UDI-DI 00886385015019

JWJ Prescription
10
510(k) clearances
497
Adverse events
0
Recalls
38
Facilities

Description

Wrist Instrument Carpal Trial, Small

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.