FDA 510(k)

ACRY TEMP

K-Number: K771257 · 1977-07-15

Decision Date1977-07-15

Product CodeEBG

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

ACRY TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Interstate Dental Co., Inc.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K771257. 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 ACRY TEMP?

ACRY TEMP is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Interstate Dental Co., Inc.. The 510(k) number is K771257.

When did ACRY TEMP receive FDA 510(k) clearance?

ACRY TEMP received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771257.

Who is the listed applicant for ACRY TEMP?

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

What is the FDA product code for ACRY TEMP?

The FDA product code for ACRY TEMP is EBG.

Other records listing Interstate Dental Co., 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.

K771248SILICONE IMPRESSION MATEOIAL

Related Devices (Code: EBG)

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 Exportação K243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.