Moe
Country not established
- Devices
- 6
What Moe makes
Moe manufactures biofeedback devices for physiological monitoring, including systems for electromyography (EMG), thermal monitoring (TMG), electroencephalography (EEG), and infrared reception. Products include specialized sensors (e.g., ultra-low noise EMG and EEG modules), peripheral interface units, and light-based feedback accessories. These devices are designed for clinical and research applications to measure muscle activity, brainwave patterns, and thermal responses.
The company’s portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database, indicating their compliance with U.S. regulatory requirements. Moe is based in the United States.
Catalogue
Biofeedback TMG1, 4, BIO1, PA1, 2, BA1/BA30 Ref K884850
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Biofeedback Device TG3, TG4 Ref K884851
Regimes: 510(k) Registry: 510(k)Biofeedback EEG1/2, Eeg Ultra Low Noise, SYC1 Ref K884853
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Moe have in the registry?
The registry currently lists 6 devices for Moe. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moe's devices?
Among its 6 most recently registered devices, Moe has devices listed in FDA 510(k) (6 devices).
What risk classes do Moe's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Moe's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Moe in the registry?
The most recently registered devices listed for Moe include BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30, BIOFEEDBACK DEVICE ACCESS. PI1, 2, 3, 4, 5/LIGHT BAR, BASIC BIOFEEDBACK, TMG4.1, SA1/2, EEG4/5, IR RECEIV and BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI..