X-Nav Technologies, LLC
X-Nav Technologies, LLC holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2026, with 4 FDA device recalls on record.
Top product codes for X-Nav Technologies, LLC
FDA recalls by X-Nav Technologies, LLC
- Z-1392-2024 — X-Guide Handpiece Adaptor Sleeve 1, Model P010701
- Z-1393-2024 — X-Guide Handpiece Adaptor Sleeve 3, Model P010727
- Z-0222-2023 — X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673
- Z-1391-2016 — X-Guide Surgical Navigation System, X-Clip Bulk Kit The X-Guide Surgical Navigation System is a computerized navigational system intended to provide assistance in both the preoperative planning phase and the intra-operative surgical phase of dental implantation procedures.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by X-Nav Technologies, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.