FDA applicant

Tekno Medical Optik-Chirurgie GmbH & Co.

Tuningen, B.W., DE2 decisions2001–20020 recalls

FDA records 2 decisions for Tekno Medical Optik-Chirurgie GmbH & Co. (Tuningen, B.W., DE) from 2001 to 2002: 2 510(k) clearances. Most are in product codes HDA (Forceps, Obstetrical) and GEI (Electrosurgical, Cutting & Coagulation &…). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Tekno Medical Optik-Chirurgie GmbH & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tekno Medical Optik-Chirurgie GmbH & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tekno Medical Optik-Chirurgie GmbH & Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Tekno Medical Optik-Chirurgie GmbH & Co.’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 “Tekno”

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

Tekno-Medical 1

Tekno Medical Optik-Chirurgie GmbH & Co.

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?

Other applicant names beginning “Tekno”