Kavo Dental Technologies, LLC
Kavo Dental Technologies, LLC holds FDA 510(k) medical device clearance, cleared in 2017, with 2 FDA device recalls on record.
Top product codes for Kavo Dental Technologies, LLC
FDA recalls by Kavo Dental Technologies, LLC
- Z-1387-2019 — DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is intended to acquire dental intraoral radiographic images. The DEXIS / KaVo sensor shall be operated by healthcare professionals, who are educated and competent to perform the acquisition of dental intra-oral radiographs. The DEXIS / KaVo sensor can be used either in combination with special positioning devices to facilitate positioning and alignment with the x-ray beam or it may also be positioned by hand with the assistance of the patient.
- Z-1101-2019 — cone-beam CT system
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 Kavo Dental Technologies, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.