FDA 510(k)

TEMP-FILL

K-Number: K812532 · 1981-10-14

Decision Date1981-10-14

Product CodeEMA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

TEMP-FILL is the device name listed in this FDA 510(k) record. The listed applicant is Madrid Uso, Jr., D.D.S.. It received FDA 510(k) clearance on 1981-10-14 under 510(k) number K812532. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP-FILL?

TEMP-FILL is a medical device that received FDA 510(k) clearance on 1981-10-14. The listed applicant is Madrid Uso, Jr., D.D.S.. The 510(k) number is K812532.

When did TEMP-FILL receive FDA 510(k) clearance?

TEMP-FILL received FDA 510(k) clearance on 1981-10-14, under 510(k) number K812532.

Who is the listed applicant for TEMP-FILL?

The FDA 510(k) record lists Madrid Uso, Jr., D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP-FILL?

The FDA product code for TEMP-FILL is EMA.

Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-Pak K261166DIA-CEMDiaDent Group International K254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, Inc.

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.