FDA Device Intelligence
HomeASPIRE BARIATRICS, INC. › AspireAssist Connector-US

AspireAssist Connector-US

ASPIRE BARIATRICS, INC. · Model 200-0019-US · UDI-DI 10857808005488

OYF Prescription
0
510(k) clearances
6
Adverse events
0
Recalls
1
Facilities

Description

Connector-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.