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Infrared Hematoma Detector

FDA product code OPT · Class 2 · Ophthalmic

3
Registered devices
2
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Infrascanner — INFRASCAN, INC.Infrascanner — INFRASCAN, INC.KIMTECH — Ansell Healthcare Product

Recent recalls

DateFirmReason
2013-10-16Cutera, Inc.Cutera received two adverse events associated with the edge of the electrode, when it was pressed against neck skin over the thyroid cartilage and due to the ab

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