510(k) K810266

Device
ETCHING GEL
Applicant
ESPE-PREMIER SALES CO.
510(k) number
K810266
Product code
EJK  
Decision
Substantially Equivalent (SESE)
Decision date
1981-02-23
Date received
1981-02-02
Regulation
872.3250
Classification name
Liner, Cavity, Calcium Hydroxide
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EJK  

510(k)DeviceApplicantDecision date
K253248Bright Cavity LinerDmp Dental Industry S.A.2026-01-13
K2302703M™ VitCal Liner/Base3M Espe Dental Products2023-02-06
K212475Prevest Denpro Cavity Liners (Apacal ART, Cal LC, Calcigel, CalUltra)Prevest Denpro Limited2022-05-13
K201799CleaniCalMaruchi2021-02-12
K202413LC ResinCal PCS&C Polymer Silicon- Und Composite Spezialitaten GmbH2020-11-20
K191103Parkell Desensitizer GelParkell, Inc.2019-11-22
K180344TheraCal DCBisco, Inc.2018-04-05
K143292TheraCal DCBisco, Inc.2015-08-04
K150559Life Fast Set, Life Regular SetSybron Dental Specialties2015-06-19
K141047LC CALCIUMHYDROXIDE LINERS&C Polymer Silicon- Und Composite Spezialitaeten2015-04-14
K134022BASE ITSpident Co., Ltd.2014-06-11
K131068TEETHMATE DESENSITIZER SET; TEETHMATE DESENSITIZER POWDER; TEETHMATE DESENSITIZER LIQUIDKuraray Noritake Dental, Inc.2013-08-27
K122421TEETHMATE DESENSITZER SET TEETHMATE DESENSITIZER POWDER TEETHMATE DESENSITIZER LIQUIDKuraray Noritake Dental, Inc.2012-12-11
K120003NUCALPulpdent Corporation2012-04-05
K113711LIME-LITE IIPulpdent Corporation2012-03-05

Legacy Summary

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FDA Review

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