Company profileCore BCI
g.tec medical engineering
An Austrian maker of complete BCI systems and of the amplifiers much of the field's research is recorded with, in business since 1999.
- Location
- Schiedlberg, Austria
- Founded
- 1999
- Class
- Core BCIAlso: Enabling technologySells complete non-invasive BCI systems for rehabilitation, assessment and communication, which is why it is counted as a BCI company. It is also one of the field's main suppliers of amplifiers, electrodes and real-time software for research, and it has an FDA-cleared system, cortiQ, that maps the cortex from ECoG recordings for the surgical team.
- Also known as
- g.tec medical engineering GmbH · g.tec · gtec · Guger Technologies · recoveriX · Unicorn Hybrid Black · BR41N.IO
- Website
- gtec.at
- Sources last checked
- 7 Oct 2026
What they are building
Builds biosignal amplifiers, electrodes and real-time processing software for EEG and for recordings from the cortical surface, and sells BCI systems built on them: recoveriX for stroke rehabilitation, mindBEAGLE for assessing and communicating with people with disorders of consciousness, and cortiQ, which maps motor, sensory and language areas from ECoG or depth electrodes in minutes, before or during epilepsy and tumour surgery.
- Interface category
- Electroencephalography · Electrocorticography
- Signal
- EEG: Summed field potentials, blurred and attenuated by skull and scalpECoG: Local field potentials, including high-gamma activity
- Lines of work
- recoveriXNon-invasive · EEG · Recording and stimulation · Approved / clearedcortiQInvasive · ECoG · Recording · Approved / cleared
- Device
- recoveriX — EEG cap with 16 active electrodes, functional electrical stimulation of the affected limb and an on-screen avatar, both triggered when the EEG shows imagined movement
- Channels
- 16 EEG channels
- Regulatory status
- CE certified medical product, according to the company; not FDA-cleared
- Device
- cortiQ — Software and an amplifier that read high-gamma activity (60 to 170 Hz) from ECoG grids, strips or depth electrodes placed for surgery, and show which sites respond to a movement, touch or language task
- Channels
- 64, 128 or 256
- Regulatory status
- FDA 510(k) cleared as cortiQ PRO (January 2020) for evaluating intracranial EEG; CE certified, according to the company
- Main use cases
- Restore, Communicate, Monitor
Where they are clinically
Approved / cleared
Authorised by a regulator for a defined use. Always check the scope.
recoveriX is CE certified as a medical product in Europe, according to the company; we have not seen the certificate, and the FDA's database lists no clearance for it. cortiQ PRO has had FDA 510(k) clearance since January 2020 for evaluating intracranial EEG, and three of the company's amplifiers and its cortical stimulator are 510(k) cleared as well. cortiQ is an invasive line in the sense that it reads from electrodes on or in the brain; g.tec does not make those electrodes, which are placed for the surgery.
Access today
Available
Authorised and obtainable for a defined group of patients or users.
- Shown in people
- A stroke-rehabilitation system that is CE certified according to the company, and a completed 30-participant gait study. Its ECoG mapping system is FDA cleared; in a three-patient study it flagged every hand motor and sensory site that stimulation mapping found. The published evidence is mostly the company's own.
- Still an aim
- Routine clinical use of rehabilitation triggered by a BCI.
- What stands in the way
- Independent controlled trials that separate the brain-triggered feedback from ordinary therapy.
On record here: 0 peer-reviewed papers
- 24 Jan 2020US FDA — 510(k) clearance. Statistical evaluation of high-gamma activity in intracranial EEG recorded with the company's amplifier, to be read together with the original waveform. A mapping aid for the surgical team. It is not an implant and not an interface for the patient to use.
- 2019EU (notified body) — CE mark. Marketing in Europe as a medical product. Stated by the company; CE certificates are not published centrally and we have not seen this one.
Why this company matters
g.tec is the clearest case of a BCI company that an implant-centred view of the field overlooks. It has sold working BCI systems for a quarter of a century, its amplifiers are widely used in published EEG and ECoG research, and recoveriX is a certified medical product that uses a BCI as therapy: the patient imagines a movement, and stimulation and an avatar respond only when the EEG shows the attempt. That is a narrower claim than restoring communication through an implant, and it is one that already reaches patients. cortiQ takes the same signal processing into the operating theatre: it reads high-gamma activity from electrodes already on the cortex and shows within minutes which sites respond to a task, as a complement to stimulation mapping. It is a use of ECoG decoding that is authorised today, for the surgeon and not as an interface for the patient. Its events (the Spring School, the BR41N.IO hackathons, the BCI Award) also make it one of the field's main meeting points. The published evidence for recoveriX is mostly the company's own research; larger independent trials would settle how much of the benefit is specific to the brain-triggered feedback.
Key milestones
2 Apr 2026
BrainSTEP, a study of gait rehabilitation after stroke with 30 participants, reaches primary completion.
2 Aug 2021
A case report from a hospital group describes language mapping with cortiQ during the removal of a glioma in one patient.
24 Jan 2020
FDA clears cortiQ PRO through the 510(k) route, for the statistical evaluation of high-gamma activity in intracranial EEG.
2020
The annual BCI & Neurotechnology Spring School begins.
2020
A feasibility study of BCI treatment for upper-limb rehabilitation after stroke is published by the company's researchers.
2019
Medical approvals for recoveriX and cortiQ; the Unicorn Hybrid Black headset for developers is introduced.
2017
Starts the BR41N.IO series of BCI hackathons.
Jun 2015
Study in three patients with epilepsy sets cortiQ's real-time mapping against electrical stimulation mapping: sensitivity 100% and specificity 80% for hand motor sites. The company's researchers are among the authors.
2007
Introduces intendiX, a P300 speller for use at home.
1999
Founded in Austria by Christoph Guger and Günter Edlinger; presents a motor-imagery BCI system the same year.
Leadership
Christoph Guger
Co-founder and co-CEO
Günter Edlinger
Co-founder and co-CEO
As publicly stated by the organisation. Not a complete list.
Competitive context
EEGApproved / cleared
Kandu
Maker of IpsiHand, a non-invasive BCI for hand rehabilitation after stroke that the FDA authorised for marketing in 2021, years before any implanted system.
sEMGNon-medical
BrainCo
Non-invasive neural interfaces sold as products: bionic limbs and EEG wearables.
IntracorticalFeasibility
Blackrock Neurotech
Maker of the electrode arrays behind most human intracortical BCI research.
ECoGFirst-in-human
CorTec
A fully implanted closed-loop system that both records from and stimulates the cortical surface.
Sources
- 01
g.tec's 25 years of neurotechnology history (opens in a new tab)
Company reportedg.tec medical engineeringChecked against source 5 Oct 2026
The company's own timeline: founding in 1999, product years, branch offices, the hackathon series from 2017 and the Spring School from 2020. It says medical approvals for cortiQ and recoveriX came in 2019 without naming the certificates.
- 02
recoveriX neurorehabilitation: product description (opens in a new tab)
Company reportedg.tec medical engineeringChecked against source 5 Oct 2026
Product page. Calls recoveriX a CE certified medical product, describes the motor-imagery, avatar and stimulation loop and a course of 25 sessions. Does not mention the FDA.
- 03
g.tec: cortiQ rapid cortical mapping, product page (opens in a new tab)
Company reportedg.tec medical engineeringChecked against source 7 Oct 2026
The company's description: passive mapping from high-gamma activity (60 to 170 Hz) recorded with ECoG grids and strips or depth electrodes, with 64, 128 or 256 channels; about six minutes for four activation maps; used with electrical cortical stimulation, which confirms the result; FDA cleared and CE certified.
- 04
g.tec medical engineering: products and community (opens in a new tab)
Company reportedg.tec medical engineeringChecked against source 5 Oct 2026
Lists the amplifier, electrode, stimulator and software lines, the Unicorn developer kits and the complete systems (recoveriX, cortiQ, mindBEAGLE), and the company's events. Audience figures on the page are the company's own.
- 05
FDA 510(k) K191432: cortiQ PRO, clearance letter and summary (opens in a new tab)
Regulatory sourceUS Food and Drug Administration24 Jan 2020Checked against source 7 Oct 2026
Read in full. Class II, regulation 21 CFR 882.1400 (electroencephalograph). Indications: to statistically evaluate brain activity reflected in a broad band of high-gamma frequencies, always interpreted together with the original waveform, for intracranial EEG recorded with the g.HIamp. The decision date is from the FDA's 510(k) database.
- 06
FDA 510(k) database: clearances held by g.tec medical engineering (opens in a new tab)
Regulatory sourceUS Food and Drug Administration (openFDA)Checked against source 7 Oct 2026
Six clearances on 7 October 2026: g.USBamp (K060803, 2006), g.HIamp (K123255, 2012), g.Nautilus PRO (K171669, 2017), g.Estim PRO (K173684, 2018), cortiQ PRO (K191432, 2020) and g.Estim FES (K200088, 2020). None is for recoveriX.
- 07
Peer reviewedJournal of Clinical NeurophysiologyJun 2015Checked against source 7 Oct 2026
DOI 10.1097/WNP.0000000000000131. Figures read from the PubMed abstract: three patients; against electrical stimulation mapping, sensitivity 100% and specificity 79.7% for hand motor sites, 100% and 73.9% for hand sensory sites. The first author's affiliation is g.tec; the patients were at Florida Hospital for Children.
- 08
Peer reviewedFrontiers in Neurology2 Aug 2021Checked against source 7 Oct 2026
DOI 10.3389/fneur.2021.652401. One patient: language sites mapped with the system from listening tasks during tumour surgery. Read from the PubMed abstract.
- 09
Peer reviewedFrontiers in Neuroscience2020Checked against source 5 Oct 2026
DOI 10.3389/fnins.2020.591435. Citation confirmed against the PubMed record. The last author is a founder of the company whose system was studied. We quote no figure from it.
- 10
Clinical registryClinicalTrials.govChecked against source 5 Oct 2026
Sponsor g.tec medical engineering GmbH. Completed with 30 participants at one site in Austria; primary completion 2 April 2026.