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Graduated electronic decelerator

Electrical torture device

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Through United Nations and Civil and political rights

Matthew Israel created the GED to replace the older punishments of spankings, pinches, and muscle squeezes, but continued to use restraints, sensory deprivation, and the withholding of food. These older punishments were often used in combination with the GED: For example, a student could be restrained to a board and then given several GED shocks in succession. While the school advertises its behavior modification program as safe, effective, and backed by science, these claims are disputed by independent experts, and the device has been condemned as a form of torture.

History

The GED was created by Matthew Israel, the founder of Judge Rotenberg Center. Before it made use of electric shocks, the school used pinches, spankings, muscle squeezes, and a wide variety of other methods of aversive intervention including punitive restraints, sensory deprivation, and the withholding of food. Matthew Israel said that the school moved to electric shocks because “A lot of injuries were occurring” and also because it is more consistent. After the school began to use electric shocks as punishment, it phased out pinches, spankings, and muscle squeezes, but retained most other aversion interventions which were used alongside, and sometimes at the same time as, the electric shocks. For example, it was a common punishment to apply multiple GED shocks while the subject was restrained.

The GED is based on the Self-Injurious Behavior Inhibiting System (SIBIS), a controversial device that delivered electric shocks to the skin for the purpose of inhibiting self-harming behavior. The SIBIS delivers a weak skin shock that lasts 0.2 seconds. The JRC used the SIBIS on 29 students between 1988 and 1990, but, in some cases, the shock was not powerful enough to produce compliance. Matthew Israel reported that one student was shocked by the SIBIS over 5,000 times in a day without producing the desired change in behavior. Israel asked the manufacturer of the SIBIS, Human Technologies, to build a device that delivered stronger shocks, but they refused. Israel then designed the GED-1, which could deliver a much more powerful shock than the SIBIS, that would last ten times as long. In 1994, the United States Food and Drug Administration (FDA) cleared the device for the treatment of self-harming behavior, as they considered it "substantially equivalent" to the SIBIS.

By 1992, Matthew Israel had also designed and deployed the GED-3a and GED-4. These new GEDs were built to deliver much more powerful shocks than the original GED-1, and were never cleared for use by the FDA. Israel stated that he created the more powerful devices "Because some students had adapted to the [GED-1]".

In 2000, the FDA incorrectly notified the JRC that it qualified for exemption from registration of the GED-3a and GED-4. When the FDA recognized this error in 2011, it notified the JRC that the devices were not approved for use and ordered that they stop using them. The JRC ignored the FDA's demands and continued to use the devices until they were banned in 2020. At the time of the ban, the GED-3a and GED-4 were the only versions of the GED in use at the center.

The use of the device was condemned as torture by the United Nations. The use of the GED has been condemned by human rights groups and disability rights organizations. In 2020, it became the third device ever banned by the FDA in the history of the organization.

In 2021, a federal court found that the FDA ban was an "inappropriately promulgated rule". The FDA rule was a ban on using these devices to treat violent or self-injurious behaviors, while not banning the device for "other purposes". A three-judge panel of the U.S. Court of Appeals for the D.C. Circuit found that this was an overstep of its authority, as it cannot regulate the practice of medicine. In 2023, Congress amended the Federal Food, Drug, and Cosmetic Act, expanding the FDA's authority and allowing them to ban a medical device for a particular use, irrespective of any other approved use. The FDA proposed a new ban based on its expanded authority in March 2024 and accepted public comments on the proposal through May 2024. As of July 2026, the agency has not acted on its proposal, despite previous self-imposed deadlines of October 2025 and May 2026. In a May 2026 statement to Disability Scoop, United States Department of Health and Human Services spokesperson Andrew Nixon said the FDA was still considering comments received. An unnamed government spokesperson did not respond to a June 2026 request for comment submitted by a Stat reporter. In July 2026, the FDA announced a new self-imposed deadline of November 2026.

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