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LRI/Toric Markers
AURORA SURGICAL, LLC · Model AS3-502 · UDI-DI 08175700109529
3
510(k) clearances
0
Adverse events
1
Recalls
26
Facilities
Description
Toric IOL Marker
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-05-19 | Haag-Streit USA Inc | During the creation of the Lenstar LS 900 software, the ability to perform a manual adjustment of the retinal thickness measurement was not disabled for products targeted for US di |
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Get your free API keyRead the docsData 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.