FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model OP0920-991 · UDI-DI 10885403095191

HND Prescription
6
510(k) clearances
91
Adverse events
0
Recalls
161
Facilities

Description

V. Mueller KNOLLE LENS NUCLEUS SPATULA and GAUGE, 30MM LG NARROW SPATULA BLD, MARKINGS AT 5, 6 AND 7MM FROM TIP, RND HNDL

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.