FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model OS4295-009 · UDI-DI 10885403104282

GFI Prescription
6
510(k) clearances
61
Adverse events
0
Recalls
145
Facilities

Description

HIBBS OSTEOTOME BLADE 1-1/4 inches3.2CM WIDE STRAIGHT OVERALL LENGTH 9-1/2 inches24.1CM

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.