FDA applicant

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler

Istanbul, TR1 decision2020–20200 recalls

FDA records 1 decision for Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler (Istanbul, TR) in 2020: 1 510(k) clearance. All are in product code OCT (Anti Fog Solution And Accessories, Endoscopy). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler’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 — Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Turkuaz”

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

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa 3

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Turkuaz”