Stoelting Co.
Country not established
- Devices
- 4
What Stoelting Co. makes
Stoelting Co. manufactures electroencephalography (EEG) systems, including standalone and modified models like the A620 EEG and its variants, as well as dual-channel electromyography (EMG) devices such as the AT53. These products are designed for neurological and neuromuscular assessments, supporting clinical and research applications in brainwave and muscle activity monitoring.
The company’s portfolio consists of Class II medical devices, authorised through FDA 510(k) clearance. These devices are listed under the US regulatory framework and are based in the United States.
Catalogue
Modification To A620 Eeg Ref K012011
Regimes: 510(k) Registry: 510(k)At 62 Eeg (A.K.A The A;pha-Theta Trainer) Ref K965006
Regimes: 510(k) Registry: 510(k)A620 Eeg Ref K944615
Regimes: 510(k) Registry: 510(k)AT53 Dual Channel Emg Ref K952797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stoelting Co. have in the registry?
The registry currently lists 4 devices for Stoelting Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stoelting Co.'s devices?
Among its 4 most recently registered devices, Stoelting Co. has devices listed in FDA 510(k) (4 devices).
What risk classes do Stoelting Co.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Stoelting Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stoelting Co. in the registry?
The most recently registered devices listed for Stoelting Co. include MODIFICATION TO A620 EEG, AT 62 EEG (A.K.A THE A;PHA-THETA TRAINER), A620 EEG and AT53 DUAL CHANNEL EMG.