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FDA 510(k)

TEMP. ACRYLIC

K-Number: K772211 · 1977-12-22

ApplicantLactong Corp.
Decision Date1977-12-22
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEMP. ACRYLIC is the device name listed in this FDA 510(k) record. The listed applicant is Lactong Corp.. It received FDA 510(k) clearance on 1977-12-22 under 510(k) number K772211. 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 TEMP. ACRYLIC?

TEMP. ACRYLIC is a medical device that received FDA 510(k) clearance on 1977-12-22. The listed applicant is Lactong Corp.. The 510(k) number is K772211.

When did TEMP. ACRYLIC receive FDA 510(k) clearance?

TEMP. ACRYLIC received FDA 510(k) clearance on 1977-12-22, under 510(k) number K772211.

Who is the listed applicant for TEMP. ACRYLIC?

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

What is the FDA product code for TEMP. ACRYLIC?

The FDA product code for TEMP. ACRYLIC is EBG.

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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

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

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