510(k) Report

FDA applicant

Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim

Istanbul, TR1 decision2015–20150 recalls

FDA records 1 decision for Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim (Istanbul, TR) in 2015: 1 510(k) clearance. All are in product code HQF (Laser, Ophthalmic). 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, ophthalmic panel, where it files most

How often FDA has decided Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Emtron Elektronik VE Mekanik 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

Which product codes does it file in?

  • HQFLaser, Ophthalmic1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K133019Fiberion Ophthalmic Endolaser ProbeEmtron Elektronik VE Mekanik Sanayi VE Ticaret Lim · 2015

The one decision as Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim →