UltraPrint-Dental Temp C&B UV
K-Number: K213643 · 2022-01-14
Device Summary
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. The listed applicant is Guangzhou Heygears IMC., Inc.. The 510(k) number is K213643.
When did UltraPrint-Dental Temp C&B UV receive FDA 510(k) clearance?
UltraPrint-Dental Temp C&B UV received FDA 510(k) clearance on 2022-01-14, under 510(k) number K213643.
Who is the listed applicant for UltraPrint-Dental Temp C&B UV?
The FDA 510(k) record lists Guangzhou Heygears IMC., Inc. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Guangzhou Heygears IMC., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EBG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.