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FDA 510(k)

ENDOSOLV E

K-Number: K980633 · 1998-05-01

ApplicantSpecialites Septodont
Decision Date1998-05-01
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOSOLV E is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1998-05-01 under 510(k) number K980633. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSOLV E?

ENDOSOLV E is a medical device that received FDA 510(k) clearance on 1998-05-01. The listed applicant is Specialites Septodont. The 510(k) number is K980633.

When did ENDOSOLV E receive FDA 510(k) clearance?

ENDOSOLV E received FDA 510(k) clearance on 1998-05-01, under 510(k) number K980633.

Who is the listed applicant for ENDOSOLV E?

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

What is the FDA product code for ENDOSOLV E?

The FDA product code for ENDOSOLV E is KIF.

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Other records listing Specialites Septodont 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.

K012427PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENTK010415ISODANK982773QUICKSET LIQUID AND POWDERK982671SECURALLOYK920692SEPTOCALCINE ULTRAK915467CIMPAT S DENTAL CEMENT

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Related Devices (Code: KIF)

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.

K262050Vioseal XSpident Co., Ltd.K253909NeoPEX™ Pre-Mixed Obturation PasteNuSmile, Ltd.K261514Calcium Hydroxide Temporary Filling Material (KP-Cal)Guilin Kevin Peter Technology Co., Ltd.K261415Injectable Root Canal Sealer (KP-Root SP)Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr Corporation

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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