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Aberrometer, Ophthalmic

FDA product code NCF · Class 1 · Ophthalmic

12
Registered devices
649
Adverse events
2
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-06-30Alcon Research, Ltd.Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software cod
2017-06-30Alcon Research, Ltd.Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software cod

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.