# FDA 483 - BURTON MEDICAL - February 20, 2026

Source: https://www.keypedia.com/records/483/burton-medical/74e28dd2-016a-4846-972c-73f15518c086

> FDA 483 for BURTON MEDICAL on February 20, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: BURTON MEDICAL
- Inspection Date: 2026-02-20
- Product Type: device
- Office Name: Chicago District Office
- Summary: BURTON MEDICAL in Addison, IL, underwent an FDA inspection from February 17-20, 2026, which identified one significant observation. The firm failed to register its APEX LED Class II medical device with the Global Unique Device Identification Database. This indicates a compliance issue regarding medical device identification requirements.

## Related Documents

- [483 - 2019-10-30](https://www.keypedia.com/records/483/burton-medical/413205f2-bd32-4769-8834-672b4c07f71a)
- [483 - 2026-02-20](https://www.keypedia.com/records/483/burton-medical/d946f15f-fed9-44f8-b16e-a14eac4ba639)

## Related Officers

- [Hammam A. Abdallah](https://www.keypedia.com/people/hammam-a-abdallah/fc1ee5c3-b00c-43af-b5a3-1bdc2ad6c5d7)

Company: https://www.keypedia.com/companies/burton-medical/4cd7a15c-6124-4d31-8f3f-f3f3c5f38c08

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669