Data / Medical devices / United States / The Judge Rotenberg Educational Center, Inc.
The Judge Rotenberg Educational Center, Inc.: FDA-registered device maker in Canton, MA, United States, 1 510(k) clearance
The Judge Rotenberg Educational Center, Inc. is registered with the FDA (registration 1222743) in Canton, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 5, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1222743
- FEI number
- 1000120805
- Address
- 240 Turnpike ST., Canton, MA, United States, 02021
- Owner or operator
- THE JUDGE ROTENBERG EDUCATIONAL CENTER, INC. (9003264)
- Roles
- Manufacturer
- First device listed
- December 11, 2007
- Registered through
- 2026
- Brand names listed
- Graduated Electronic Decelerator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Aversive Conditioning | HCB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 5, 1994 | K911820 | GED (GRADUATED ELECTRONIC DECELERATOR | HCB | Substantially Equivalent | Behavior Research Institute, Inc. | accessdata.fda.gov |
Updated December 5, 1994. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.