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FDA 510(k)

Digital Temp

K-Number: K242559 · 2024-11-26

ApplicantSprintray, Inc.
Decision Date2024-11-26
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Digital Temp is the device name listed in this FDA 510(k) record. The listed applicant is Sprintray, Inc.. It received FDA 510(k) clearance on 2024-11-26 under 510(k) number K242559. 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 Digital Temp?

Digital Temp is a medical device that received FDA 510(k) clearance on 2024-11-26. The listed applicant is Sprintray, Inc.. The 510(k) number is K242559.

When did Digital Temp receive FDA 510(k) clearance?

Digital Temp received FDA 510(k) clearance on 2024-11-26, under 510(k) number K242559.

Who is the listed applicant for Digital Temp?

The FDA 510(k) record lists Sprintray, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Temp?

The FDA product code for Digital Temp is EBG.

Other records listing Sprintray, 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.

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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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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.

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