DANNORITZER Medizintechnik GmbH & Co. KG

Country not established

Devices: 2,001
FDA recalls: 1

What DANNORITZER Medizintechnik GmbH & Co. KG makes

DANNORITZER Medizintechnik GmbH & Co. KG manufactures spinal rongeurs, including the DANmed line, as well as monopolar laparoscopic accessories for surgical procedures.

These devices are classified as Class II under regulatory frameworks, with submissions recorded in the FDA’s 510(k) and UDI registries. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Company details

DUNS number: 314648911
Email: [email protected]
Phone: +497461962390

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by DANNORITZER Medizintechnik GmbH & Co. KG, initiated on 2018-08-06. By recorded status: 1 terminated. The reasons filed fall into these groups: labeling or instructions for use and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

2017 0
2018 1
2019 0
2020 0
2021 0
2022 0
2023 0
2024 0
2025 0
2026 0

2018
- 6 Aug 2018 Z-0062-2019 Class III Terminated The Manual cleaning process and the usability of the reprocessing instruction by the user had not been validated. The IFU was modified to remove the manual cleaning method and revised the instructions for use for clarity and readability. Distribution: US Nationwide in the States of OH, MI, MA, CA, OK, TN, GA, FL, IL, NC, TX, MO. Submission number: K052759