Inomed Medizintechnik GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242852 | ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. | June 13, 2025 |
| K233292 | ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress | October 27, 2023 |
| K223254 | C2 Xplore | January 27, 2023 |
| K212164 | Mapping Suction Probe | November 11, 2022 |
| K212166 | ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress | January 7, 2022 |
| K152505 | C2 NerveMonitor System | February 1, 2016 |
| K111647 | C2 NERVEMONITOR SYSTEM WITH ACCESSORIES | October 6, 2011 |
| K091874 | INOMED ADHESIVE LARYNGEAL ELECTRODES, MODELS 530655, 530656 | November 18, 2009 |
| K042208 | ISIS MER SYSTEM/ELEKTA MER SYSTEM | March 18, 2005 |
| K910972 | WALTER GRAPHTEK | October 2, 1991 |