FDA applicant

Photonic Optische Gerate Gesmbh & Cokg

Vienna, AT1 decision2007–20070 recalls

FDA records 1 decision for Photonic Optische Gerate Gesmbh & Cokg (Vienna, AT) in 2007: 1 510(k) clearance. All are in product code FFS (Image, Illumination, Fiberoptic, For Endoscope). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Photonic Optische Gerate Gesmbh & Cokg’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Photonic Optische Gerate Gesmbh & Cokg by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Photonic Optische Gerate Gesmbh & Cokg’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 “Photonic”

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

Photonic Optische Gerate GmbH & Cokg 1

Photonic Optische Gerate Gesmbh & Cokg

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Photonic”