UltraPrint-Dental Temp C&B UV
K-Number: K213643 · 2022-01-14
ApplicantGuangzhou Heygears IMC., Inc.
Decision Date2022-01-14
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
UltraPrint-Dental Temp C&B UV is a medical device manufactured by Guangzhou Heygears IMC., Inc.. It received FDA 510(k) clearance on 2022-01-14 under approval number K213643. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the UltraPrint-Dental Temp C&B UV?
UltraPrint-Dental Temp C&B UV is a medical device that received FDA 510(k) clearance on 2022-01-14. It is manufactured by Guangzhou Heygears IMC., Inc.. The 510(k) number is K213643.
When was UltraPrint-Dental Temp C&B UV approved by the FDA?
UltraPrint-Dental Temp C&B UV received FDA 510(k) clearance on 2022-01-14, under approval number K213643.
What company makes UltraPrint-Dental Temp C&B UV?
UltraPrint-Dental Temp C&B UV is manufactured by Guangzhou Heygears IMC., Inc..
What is the FDA product code for UltraPrint-Dental Temp C&B UV?
The FDA product code for UltraPrint-Dental Temp C&B UV is EBG.
Other Devices by Guangzhou Heygears IMC., Inc.
Related Devices (Code: EBG)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.