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Atlas
Eyoto, Inc. · Model Global · UDI-DI 05070000542829
10
510(k) clearances
5
Adverse events
1
Recalls
66
Facilities
Description
Automated AC powered Ophthalmic Lens Analyser for use in the testing and verification of semi finished and finished unmounted ophthalmic lenses
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-08-06 | Carl Zeiss Meditec AG | Due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety |
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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.