Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

UltraPrint-Dental Temp C&B UV

K-Number: K213643 · 2022-01-14

Decision Date2022-01-14
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UltraPrint-Dental Temp C&B UV is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Heygears IMC., Inc.. It received FDA 510(k) clearance on 2022-01-14 under 510(k) 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. 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.