FDA applicant

Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi

Ankara, TR1 decision2024–20240 recalls

FDA records 1 decision for Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi (Ankara, TR) in 2024: 1 510(k) clearance. All are in product code FGB (Ureteroscope And Accessories, Flexible/Rigid). 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 Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Elmed Elektronik VE Medikal Sanayi VE…’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 “Elmed”

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

Elmed, Inc. 27 Elmed USA 1

Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Elmed”