FDA Device Intelligence
Home › Asensus Surgical, Inc. › Senhance

Senhance

Asensus Surgical, Inc. · Model X9007630 · UDI-DI 00815440021115

Prescription
0
510(k) clearances
0
Adverse events
0
Recalls
0
Facilities

Description

Senhance System Power Pack (US)

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.