Dental Device Guide
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Manufacturer registered with FDA

Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi ve Ticaret Anon

Izmir, Türkiye. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10056145Manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Türkiye

Devices listed with FDA

What Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi ve Ticaret Anon currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker
Nucleoss
2021
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
Nucleoss
2021

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

Also lists devices cleared under other names

Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi ve Ticaret Anon lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST (1).

Decided510(k)DeviceApplicantDevice type
27 Aug 2020K192062Nucleoss T6 Dental Implant SystemSanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. STDZE Root-Form Endosseous Implant

Registered establishments

EstablishmentLocationWhat it does
SANLILAR TIBBI CIHAZLAR MEDIKAL KIMYA SANAYI TICARET LIMITED SIRKETIFDA reg. 3014112268Izmir, TürkiyeManufacturer

Other names on FDA records

Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Limited Sirketi

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10056145). 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.