510(k) Report

FDA applicant

Morcher GmbH

Stuttgart1 decision2003–20030 recalls

FDA records 1 decision for Morcher GmbH (Stuttgart) in 2003: 1 original PMA approval. All are in product code MRJ (Ring, Endocapsular). 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 Morcher GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Morcher GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Morcher GmbH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Morcher GmbH’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?

  • MRJRing, Endocapsular1decision

What has FDA decided for it lately?

  • P010059Morcher Capsular Tension Ring, Types 14, 14A and 14CMorcher GmbH · 2003

The one decision as Morcher GmbH →