FDA Device Intelligence
Home › STRYKER CORPORATION › XprESS Ultra

XprESS Ultra

STRYKER CORPORATION · Model MSB&LLF · UDI-DI 00857326005123

PNZLRC Prescription
9
510(k) clearances
30
Adverse events
0
Recalls
15
Facilities

Description

ENT Dilation System 6x20mm

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.