Neuralink, a tech startup co-founded by Elon Musk, has received approval from the United States Food and Drug Administration FDA to test its brain implant on human beings.
This was announced in a statement shared via the company’s official Twitter page on Thursday
Recommended News:
- Atiku reacts as supreme court dismisses suit against Shettima, awards penalty
- Nigerians call on Dapo Abiodun to immortalise late 24yr old Abass Oyeyemi (Video)
- Lagos governor celebrates Tinubu over national honour, handover
- Aero Contractors CEO counters FG, says Nigeria Air cannot start operations by May 29
“We are excited to share that we have received the FDA’s approval to launch our first-in-human clinical study!” the tweet read. “This is the result of incredible work by the Neuralink team in close collaboration with the FDA and represents an important first step that will one day allow our technology to help many people.”
Musk also commented on the post on Friday, tweeting, “Congratulations to the Neuralink team.”
Congratulations Neuralink team! https://t.co/AWZGf33UDr
— Elon Musk (@elonmusk) May 26, 2023
The implants are meant to allow humans to interface directly with computers. Musk had earlier touted the product as a possible solution for persons living with disabilities, as it could help restore vision and movement. He made headlines late last year after stating that he trusted the device enough to implant them in his children.
Already, the coin-sized implants have been tested on monkeys and pigs.
During a presentation by the company in December last year, Neuralink showed several monkeys playing basic video games or moving a cursor on a computer screen using Neuralink chips implanted in their brains, CBS News reports.
Musk, who also spoke at the presentation said, “We would initially enable someone who has almost no ability to operate their muscles and enable them to operate their phone faster than someone who has working hands.
“As miraculous as it may sound, we are confident that it is possible to restore full body functionality to someone who has a severed spinal cord.”
Employees told Reuters in March the company had earlier sought approval from the FDA in 2022 but the application was rejected. The regulator cited several concerns including the safety of lithium battery powering the device, possibility of the chip’s wires migrating within the brain, and the challenge of safely removing the device without damage to the brain.
Neuralink is currently under several federal investigations including an inquiry by the US Department of Agriculture, into potential animal-welfare violations during the animal tests conducted by the company.
