Data / Medical devices / Germany / MIPM Mammendorfer Institut fur Physik und Medizin GmbH
MIPM Mammendorfer Institut fur Physik und Medizin GmbH: FDA-registered device maker in MAMMENDORF/MUNICH Bavaria, Germany, 4 510(k) clearances
MIPM Mammendorfer Institut fur Physik und Medizin GmbH is registered with the FDA (registration 8043459) in MAMMENDORF/MUNICH Bavaria, Germany. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated October 21, 2025. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 8043459
- FEI number
- 3004117725
- Address
- Oskar-von-Miller Str. 6-7, MAMMENDORF/MUNICH Bavaria, Germany, 82291
- Owner or operator
- MIPM Mammendorfer Institut fur Physik und Medizin GmbH (9001715)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 6, 2015
- Registered through
- 2026
- Brand names listed
- MMG Sensor for Neuromuscular Transmission Monitor TOF3D, MRI Patient Monitor TeslaDUO, MRI Patient Monitoring System Tesla M3, Neuromuscular Transmission Monitor NT 100, Neuromuscular Transmission Monitor TOF3D, SpaceStation MRI, Tesla DUO, TeslaM3 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Pump, Infusion | MRZ | 2 | Contract manufacturer | accessdata.fda.gov |
| Electrode, Electrocardiograph | DRX | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Peripheral, Electric | KOI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 21, 2025 | K250887 | Neuromuscular Transmission Monitor TOF3D (2510091) | KOI | Substantially Equivalent | MIPM Mammendorfer Institut für Physik und Medizin GmbH | accessdata.fda.gov |
| May 5, 2022 | K212434 | Neuromuscular Transmission Monitor TOF3D | KOI | Substantially Equivalent | MIPM Mammendorfer Institut für Physik und Medizin GmbH | accessdata.fda.gov |
| June 28, 2016 | K153739 | MRI Patient Monitor TeslaDUO | MWI | Substantially Equivalent | Mipm Mammendorfer Institut Fur Physik Und Medizin | accessdata.fda.gov |
| May 7, 2015 | K142032 | MRI PATIENT MONITORING SYSTEM TESLA M3 | MWI | Substantially Equivalent | Mipm Mammendorfer Institut Fur Physik Und Medizin | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Peripheral, Electric
- All makers of Electrode, Electrocardiograph
- All makers of Accessories, Pump, Infusion
- All makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Updated October 21, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.