Atlas FDA

X-NAV Technologies, LLC

3 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch X-NAV Technologies, LLC

RecordFirmDate
X-Guide Handpiece Adaptor Sleeve 1, Model P010701 recall (Z-1392-2024)X-NAV Technologies, LLC2024-03-29
X-Guide Handpiece Adaptor Sleeve 3, Model P010727 recall (Z-1393-2024)X-NAV Technologies, LLC2024-03-29
X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or per recall (Z-0222-2023)X-NAV Technologies, LLC2022-11-10

Track X-NAV Technologies, LLC automatically

Every clearance here is in the API, with alerts when new ones post.