FDA Device Intelligence
Home › Alcon Laboratories, Inc. › SILIKON

SILIKON

Alcon Laboratories, Inc. · Model 8065601185 · UDI-DI 00380656011859

LWL Prescription
1
510(k) clearances
223
Adverse events (3 deaths)
0
Recalls
6
Facilities

Description

SILIKON 1000 8.5ML VIAL Purified polydimethylsiloxane

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.