510(k) Report

FDA applicant

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

Bolgesi Tekeli, TR1 decision2017–20170 recalls

FDA records 1 decision for Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti (Bolgesi Tekeli, TR) in 2017: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 4 predicates, 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 Med. Kim.San.Tic.Ltd.Sti’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Sanlilar Tibbi Cihazlar Med. Kim.San.Tic.Ltd.Sti by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Sanlilar”

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