510(k) K002302

Device
SUPER 14
Applicant
DENTAL ALLOY PRODUCTS, INC.
510(k) number
K002302
Product code
EJH  
Decision
Substantially Equivalent (SESE)
Decision date
2000-09-26
Date received
2000-07-28
Regulation
872.3710
Classification name
Alloy, Metal, Base
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Related Records

Applicant Contact

Contact
RODNEY GUYTON
Address
1190 Mahalo Pl. Compton CA US 90220 90220

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EJH  

510(k)DeviceApplicantDecision date
K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO2013-03-14
K040180CONTINUM VAalba Dent, Inc.2004-03-04
K040179CONTINUMAalba Dent, Inc.2004-03-03
K033356VERASOFT ESAalba Dent, Inc.2003-12-30
K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.2003-12-23
K032136WIROBOND CBego U.S.A.2003-09-04
K031627NANO-TICROWNNano-Write Corp.2003-06-11
K030632PD CASTA-HMountain Medico, Inc.2003-05-07
K030416CERACAST-VMountain Medico, Inc.2003-04-14
K030161SUPERBONDAmerican Dent-All, Inc.2003-03-17
K024214KAVO EVEREST TITANBLANKKavo America2003-03-12
K023499GOLD CORE PLUSPentron Laboratory Technologies2003-01-13
K023502JEWEL CAST PLUSPentron Laboratory Technologies2002-12-18
K023477BIOLOYNeirynck & Vogt NV2002-12-13
K021971CERALOYNeirynck & Vogt NV2002-08-01

Legacy Summary

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FDA Review

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