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Instrument, Measuring, Corneal Radius

FDA product code HJB · Class 1 · Ophthalmic

87
Registered devices
22
Adverse events
2
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-11-14Haag-Streit USA IncCurrently there is a possibility, at the start of the perimetry examination, for the background illumination of the cupola not to turn on. If no illumination
2011-06-20Haag-Streit USA IncA patient record may be linked to an incorrect/inconsistent set of calculation results under specific circumstances when using EyeSuite Software version i2.000.

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