FDA Device Intelligence
Home › Elite Manufacturing › Elite

Elite

Elite Manufacturing · Model STA · UDI-DI 00840191000133

INW
10
510(k) clearances
15
Adverse events (2 deaths)
1
Recalls
103
Facilities

Recalls

DateFirmReason
2003-05-30Chattanooga Corp.Product contains an improper bracket for the transducer.

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.