FDA applicant

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa

San Francisco, CA3 decisions2011–20154 recalls

FDA records 3 decisions for Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa (San Francisco, CA) from 2011 to 2015: 3 510(k) clearances. Most are in product codes MUI (Media, Coupling, Ultrasound) and NUC (Lubricant, Personal). Its devices cite 2 predicates, 0 of them its own earlier devices. 4 recalls are linked to its devices.

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

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

How often FDA has decided Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

4in 2023

2011high 4 (2023) · low 0 (2011)2026

Class I Class II/III not classified

FIG. 1 — Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Turkuaz Saglik Hizmetleri Medikal…’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 “Turkuaz”

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

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal… 1

Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Turkuaz”