FDA applicant

Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST

Izmir, TR1 decision2020–20200 recalls

FDA records 1 decision for Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST (Izmir, TR) in 2020: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sanlilar Tibbi Cihazlar Medikal Kimya…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Sanlilar”

FDA records each applicant name separately; these may or may not be the same firm.

Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti 1

Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Sanlilar”