Ritter Dental Implant System

Implant, Endosseous, Root-form

Ritter Implants GmbH & Co. KG

The following data is part of a premarket notification filed by Ritter Implants Gmbh & Co. Kg with the FDA for Ritter Dental Implant System.

Pre-market Notification Details

Device IDK180183
510k NumberK180183
Device Name:Ritter Dental Implant System
ClassificationImplant, Endosseous, Root-form
Applicant Ritter Implants GmbH & Co. KG Gruner Weg 32 Biberach,  DE 88400
ContactWemer Schmitz
CorrespondentRaymond J Kelly
Licensale Inc. 68 Southwood Terrace Southbury,  CT  06488
Product CodeDZE  
CFR Regulation Number872.3640 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-01-23
Decision Date2019-01-24

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
ERITCOD1811 K180183 000
ERITCOD3P1 K180183 000
ERITCOD4P1 K180183 000
ERITNLCOD1811 K180183 000
ERITNLCOD181P1 K180183 000
ERITNLCOD182P1 K180183 000
ERITNLCOD1831 K180183 000
ERITNLCOD183P1 K180183 000
ERITNLCOD184P1 K180183 000
ERITNLCOD1P1 K180183 000
ERITCOD304P1 K180183 000
ERITCOD303P1 K180183 000
ERITCOD302P1 K180183 000
ERITCOD181P1 K180183 000
ERITCOD1821 K180183 000
ERITCOD1831 K180183 000
ERITCOD1841 K180183 000
ERITCOD184P1 K180183 000
ERITCOD2P1 K180183 000
ERITCOD3011 K180183 000
ERITCOD301P1 K180183 000
ERITCOD3021 K180183 000
ERITNLCOD3011 K180183 000
ERITNLCOD301P1 K180183 000
ERITCOD5P1 K180183 000
ERITCOD6P1 K180183 000
ERITNLCOD05P1 K180183 000
ERITNLCOD1821 K180183 000
ERITNLCOD1841 K180183 000
ERITNLCOD2P1 K180183 000
ERITNLCOD3021 K180183 000
ERITNLCOD3041 K180183 000
ERITNLCOD3P1 K180183 000
ERITCOD3041 K180183 000
ERITCOD3031 K180183 000
ERITCOD1P1 K180183 000
ERITNLCOD302P1 K180183 000
ERITNLCOD3031 K180183 000
ERITNLCOD303P1 K180183 000
ERITNLCOD304P1 K180183 000
ERITNLCOD4P1 K180183 000
ERITNLCOD5P1 K180183 000
ERITCOD05P1 K180183 000
ERITCOD182P1 K180183 000
ERITCOD183P1 K180183 000
ERITNLCOD6P1 K180183 000

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