FDA Device Intelligence
HomeSaeshin Precision Co., Ltd. › TRAUS ENDO

TRAUS ENDO

Saeshin Precision Co., Ltd. · Model TRAUS ENDO #3 · UDI-DI 08809260470774

EKX
10
510(k) clearances
746
Adverse events
0
Recalls
92
Facilities

Description

'10:1 TRAUS MCE10XX+TRAUS XEW10+ACL(B)-46EP

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.