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FDA 510(k)

IONOCAL

K-Number: K871562 · 1987-05-20

ApplicantForemost Dental Mfg., Inc.
Decision Date1987-05-20
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IONOCAL is the device name listed in this FDA 510(k) record. The listed applicant is Foremost Dental Mfg., Inc.. It received FDA 510(k) clearance on 1987-05-20 under 510(k) number K871562. 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 IONOCAL?

IONOCAL is a medical device that received FDA 510(k) clearance on 1987-05-20. The listed applicant is Foremost Dental Mfg., Inc.. The 510(k) number is K871562.

When did IONOCAL receive FDA 510(k) clearance?

IONOCAL received FDA 510(k) clearance on 1987-05-20, under 510(k) number K871562.

Who is the listed applicant for IONOCAL?

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

What is the FDA product code for IONOCAL?

The FDA product code for IONOCAL is EMA.

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Other records listing Foremost Dental Mfg., Inc. as applicant

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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-PakK261166DIA-CEMDiaDent Group InternationalK254109G-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.

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