FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model OS1079-002 · UDI-DI 10885403102172

GEG Prescription
10
510(k) clearances
39
Adverse events
0
Recalls
228
Facilities

Description

KEY PERIOSTEAL ELEVATOR 1/4 inches6.3MM WIDE OVERALL LENGTH 6-7/8 inches17.5CM

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.