510(k) Report

FDA applicant

Dannoritzer Medical Instruments

Hot Springs, NC1 decision2003–20030 recalls

FDA records 1 decision for Dannoritzer Medical Instruments (Hot Springs, NC) in 2003: 1 510(k) clearance. All are in product code HAE (Rongeur, Manual). 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, neurology panel, where it files most

How often FDA has decided Dannoritzer Medical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dannoritzer Medical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dannoritzer Medical Instruments’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?

  • HAERongeur, Manual1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K023868Dan Kerrison Rongeurs, Models K1 + Billy 1Dannoritzer Medical Instruments · 20031cites it

What has FDA decided for it lately?

  • K023868Dan Kerrison Rongeurs, Models K1 + Billy 1Dannoritzer Medical Instruments · 2003

The one decision as Dannoritzer Medical Instruments →

Other applicant names beginning “Dannoritzer”

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

Dannoritzer Medizintechnik GmbH & Co. KG 1