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Instrument, Measuring, Lens, Ac-Powered

FDA product code HLM · Class 1 · Ophthalmic

61
Registered devices
5
Adverse events
1
Recalls
16
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-08-06Carl Zeiss Meditec AGDue to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guarantee

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