FDA Device Intelligence
Home › Diamatrix › Diamatrix

Diamatrix

Diamatrix · Model W48 · UDI-DI 00813059017116

HNC Prescription
10
510(k) clearances
21
Adverse events
1
Recalls
190
Facilities

Description

Varley Lasik K-wire lid speculum, .039" Heavy stainless wire, Temporal, 14mm Open square blades with modified bent shafts, 30mm Blade spread, 60mm total length, Stainless

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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.