Devices

Thin-film graphene cortical surface interface from INBRAIN, used intraoperatively in a first-in-human study at Manchester. Company release; contact counts not published in the sources read.

Catalog specification sheet - Cortical surface

INBRAIN graphene cortical interface

Record ID
BTSD-STUP-0003
Reviewed
2026-10-08
Interface
ecog
Evidence stage
human

Independent, source-linked catalog sheet. Not a manufacturer-issued datasheet, regulatory decision or instructions for clinical use. Human evidence does not establish approval. Source-specific restrictions, conflicts and missing specifications are retained below.

INBRAIN graphene cortical interface

INBRAIN’s BCI is a flexible graphene thin film placed on the cortex during tumor surgery. The first four patients showed no device-related adverse events and high-gamma phoneme activity. This sheet uses company releases and the registry ID, so electrode geometry is Unreported.

Identity

FieldValue and source scope
DeviceINBRAIN Neuroelectronics graphene BCI cortical film [1][2]
ManufacturerINBRAIN Neuroelectronics, Barcelona; spin-off of ICN2 and CSIC [1][2]
Interface classCortical surface thin-film graphene electrode array [1]
OriginCompany device; first-in-human study sponsored by the University of Manchester [1]
First demonstratedFirst human application announced September 27, 2024 [2]
First human implantUnreported
Species studiedHuman [1][2]
Regulatory statusInvestigational; first-in-human study NCT06368310 [1]
FunctionBrain signal monitoring and targeted stimulation during tumor surgery; high-gamma decoding for language mapping [1]
Target tissueCortical surface during awake brain tumor surgery [1]

Geometry and architecture

FieldValue and source scope
Interface typeUltra-flexible thin-film graphene semiconductor with high-density, multiscale, bidirectional contacts and reduced graphene oxide nanoporous matrices [1]
Array layoutUnreported
Electrode countUnreported
PitchUnreported
Electrode lengthsUnreported
Shank width and thicknessUnreported
Tip and exposed site geometryUnreported
Contact coatingUnreported
InsulationUnreported
Insertion methodUnreported
Anchoring and fixationUnreported

Electrode and channel physics

FieldValue and source scope
Exposed site areaUnreported
Electrode materialUnreported
Impedance (with measurement frequency)Unreported
Noise floor or SNRUnreported
Recording modalityUnreported
Sampling rateUnreported
Stimulation capabilityUnreported
Charge injection limitUnreported
Reference and groundUnreported

Tissue interface and bioresponse

FieldValue and source scope
Target tissueUnreported
Insertion trauma and BBB disruptionUnreported
Vascular disruption riskUnreported
Micromotion sensitivityUnreported
Gliosis and encapsulationUnreported
Neuron loss near sitesUnreported
Foreign-body response mitigationUnreported
Typical failure modesUnreported

System architecture

FieldValue and source scope
Onboard electronicsUnreported
Data pathUnreported
Telemetry bandwidthUnreported
Sampling rateUnreported
PowerUnreported
Thermal managementUnreported
Packaging and hermeticityUnreported
MRI compatibilityUnreported
Surgical complexityUnreported
Output connectorsUnreported

Performance envelope

FieldValue and source scope
Acute yieldUnreported
Chronic yieldUnreported
Stability over timeUnreported
LongevityUnreported
Revision and explant experienceUnreported
Adverse eventsUnreported
Notable demonstrationsUnreported

Clinical and preclinical evidence

FieldValue and source scope
Human subjectsInterim analysis of the first four patients at the Manchester Centre for Clinical Neurosciences; the 2024 release said 8 to 10 patients were planned [1][2]
Preclinical cohortUnreported
Follow-up durationUnreported
IndicationsUnreported
Trials and registriesNCT06368310, sponsor University of Manchester; chief investigator David Coope [1]
Primary outcomesCompany-reported: no device-related adverse events in the first four patients; during awake language mapping the device captured distinct high-gamma activity linked to different phonemes [1]
Key limitationsIntraoperative, short-term use in tumor surgery. Contact counts, pitch and dimensions were not in the sources read. Company release [1][2]

Engineering tradeoffs

FieldValue and source scope
StrengthsUnreported
LimitationsUnreported
Scaling constraintsUnreported

Version boundary

The configuration in the interim analysis of July 2025. Enrolment completion was announced in April 2026 but was not reviewed here.

References

  1. INBRAIN interim analysis release, July 28, 2025.
  2. ICN2, first human application, September 27, 2024.