FDA Device Intelligence
HomeDevice types › LXC

Monitor, Pressure, Intracompartmental

FDA product code LXC · Class U · Unknown

42
Registered devices
20
Adverse events
2
Recalls
15
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-06-28MY01, INC.There is an incorrect version of the needle in the introducer part of devices. The affected Lots were manufactured using needles with a needle trocar geometry w
2005-07-22Stryker Instruments Div. of Stryker CorporationThe pressure indicated may be inaccurate, and this inaccuracy may be not detectable by the user.

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