FDA Device Intelligence
Home › AURORA SURGICAL, LLC › Scleral Depressors

Scleral Depressors

AURORA SURGICAL, LLC · Model AS14-102T · UDI-DI 08175700156110

HNX
2
510(k) clearances
11
Adverse events
0
Recalls
84
Facilities

Description

O'Connor Scleral Depressor, Titanium

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.