Dental Device Guide
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Manufacturer registered with FDA

Medicon EG

TUTTLINGEN, Germany. Lists 21 dental device types with FDA across 4 registered establishments, and holds 9 510(k) clearances as applicant.

FDA owner/operator9018008FDA owner/operator10052370FDA owner/operator10052381FDA owner/operator10052417Contract manufacturerForeign exporterManufacturer
Device types listed
21
Brands and models
2
510(k) clearances
91995–2005
Markets registered in
164,081 registrations outside the US
Establishments
4Germany
1995: 51997: 12004: 12005: 21990200020102020

510(k) clearances per year, 1990–2026

Registered in 16 markets

Where regulators' registries name Medicon EG as the manufacturer or the registration holder of a device.

All markets
United States: 21 device types listedThailand: 2,380 registrationsSouth Korea: 502 registrationsSaudi Arabia: 333 registrationsCosta Rica: 255 registrationsUnited Kingdom: 252 registrationsSerbia: 122 registrationsAustralia: 93 registrationsCanada: 71 registrationsTaiwan: 30 registrationsBrazil: 15 registrationsColombia: 10 registrationsChina: 8 registrationsIsrael: 6 registrationsHong Kong: 3 registrationsPeru: 1 registrations
RegisteredHome: GermanyOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerMedicon EG9 clearances1995–2005Below
ThailandThai FDAManufacturerMEDICON EG2,380—Pure Global AI
South KoreaMFDSManufacturerMedicon eGMEDICON eG · Medicon eG. · +25021998–2026Pure Global AI
Saudi ArabiaSFDAManufacturerMedicon eG333—Pure Global AI
Costa RicaMinisterio de SaludManufacturerMEDICON eGMedicon eG255—Pure Global AI
United KingdomMHRAManufacturerMedicon eG252—Pure Global AI
SerbiaALIMSManufacturerMEDICON eG1222022–2025Pure Global AI
AustraliaTGAManufacturerMedicon Eg932004–2025Pure Global AI
CanadaHealth CanadaRegistration holderMEDICON EG712008–2012Pure Global AI
TaiwanTFDAManufacturerMEDICON EG301988–2026Pure Global AI
BrazilANVISAManufacturerMEDICON EG152011–2020Pure Global AI
ColombiaINVIMARegistration holderMEDICON EG.10—Pure Global AI
ChinaNMPARegistration holder麦迪德致公司MEDICON eG麦迪德致公司 MEDICON eG · 麦迪德致公司Medicon eG8—Pure Global AI
IsraelAMARManufacturerMEDICON EGMEDICON eG6—Pure Global AI
Hong KongMDDManufacturerMEDICON eG32025–2025Pure Global AI
PeruDIGEMIDManufacturerMEDICON eG12014–2014Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Medicon EG currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Bone PlateJEY · Class 2Maxillofacial plates & screwsMaker—2007
Orthodontic WireDZC · Class 1Orthodontic wires & bandsMaker—1998
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker—2004
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker—2007
Orthodontic Band PusherECS · Class 1Dental hand instrumentsMaker—2002
Dental Surgical Tissue ScissorsEGN · Class 1Dental hand instrumentsMaker—1978
Periodontic ProbeEIX · Class 1Dental hand instrumentsMaker—1998
Dental Plastic Filling InstrumentEIY · Class 1Dental hand instrumentsMaker—2007
Operative ExplorerEKB · Class 1Dental hand instrumentsMaker—2007
Dental Surgical ElevatorEMJ · Class 1Dental hand instrumentsMaker—2007
Periodontic KnifeEMO · Class 1Dental hand instrumentsMaker—2002
Periodontic CuretteEMS · Class 1Dental hand instrumentsMaker—1998
Intraosseous Fixation ScrewDZL · Class 2Maxillofacial plates & screwsMaker—2017
Rubber Dam ClampEEF · Class 1Rubber dam systemsMaker—2002
All Precision AttachmentEGG · Class 1—Lister
Magnetic Inserts
2025
Dental Wax CarverEIK · Class 1Dental hand instrumentsMaker—1998
Crown RemoverEIS · Class 1Dental hand instrumentsMaker—1998
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsMaker—2007
Surgical Osteotome ChiselEMM · Class 1Dental hand instrumentsMaker—2002
Orthodontic PlierJEX · Class 1Dental hand instrumentsMaker—2002
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Medicon Epiplating System
2025

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Medicon EG as the applicant, including filings under its other names.

Decided510(k)DeviceDevice type
15 Jun 2005K050478MEDICON IMF-ORION SCREWSDZE Root-Form Endosseous Implant
23 Feb 2005K043297MEDICON 2.4 MANDIBULAR RECONSTRUCTION PLATING SYSTEMJEY Bone Plate
19 Aug 2004K041527AARHUS ANCHORAGE SYSTEMDZE Root-Form Endosseous Implant
11 Mar 1997K970256INTRAORAL MANDIBULAR DISTRACTION DEVICEJEY Bone Plate
27 Jul 1995K951689TITANIUM MANDIBULAT RECONSTRUCTION SYSTEMJEY Bone Plate
27 Jul 1995K951687MESH TITANIUM IMPLANT SYSTEMJEY Bone Plate
26 Jul 1995K951691CMS CRANIO MAXILLO FACIAL TITANIUM IMPLANT SYSTEMJEY Bone Plate
26 Jul 1995K951690TITANIUM MINIPLATE SYSTEMJEY Bone Plate
26 Jul 1995K951688MICRO TITANIUM PLATE SYSTEMJEY Bone Plate

Registered establishments

EstablishmentLocationWhat it does
Kreidler Medizintechnik GmbHFDA reg. 3003322138Wurmlingen Baden-Wurttemberg, GermanyContract manufacturer
MEDICON, E.G.FDA reg. 8010099TUTTLINGEN Baden-Wurttemberg, GermanyComplaint file establishment, Contract manufacturer, Foreign exporter, Manufacturer
Teufel & Gerlach GmbHFDA reg. 3013497507Tuttlingen Baden-Wurttemberg, GermanyContract manufacturer
Wenzler Medizintechnik GmbHFDA reg. 3002862271Frittlingen Baden-Wurttemberg, GermanyContract manufacturer

Other names on FDA records

Kreidler Medizintechnik GmbH · Teufel & Gerlach GmbH · Wenzler Medizintechnik GmbH

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9018008, 10052370, 10052381, 10052417). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.