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OYDClass II

Optical Diagnostic Device For Melanoma Detection

21 CFR 878.1820 / General, Plastic Surgery

OYD is the FDA product code for Optical Diagnostic Device For Melanoma Detection, a class II device type, regulated under 21 CFR 878.1820. FDA's definition for this code reads: "An optical diagnostic device for melanoma detection is a prescription device that measures and analyzes optical properties of a skin lesion. The device is intended for use by a physician trained in the clinical diagnosis and management of skin cancer as an adjunctive device following identification of a suspicious...". As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
OYD
Device name
Optical Diagnostic Device For Melanoma Detection
FDA definition
An optical diagnostic device for melanoma detection is a prescription device that measures and analyzes optical properties of a skin lesion. The device is intended for use by a physician trained in the clinical diagnosis and management of skin cancer as an adjunctive device following identification of a suspicious skin lesion. The output given by the device is intended to be used in combination with clinical and historical signs of skin cancer to obtain additional information prior to a decision to biopsy. It is not for use as a standalone diagnostic and is not for use to confirm a clinical diagnosis. Please reference https://www.federalregister.gov/documents/2026/03/25/2026-05772/general-and-plastic-surgery-devices-reclassification-of-optical-diagnostic-devices-for-melanoma.
Regulation
21 CFR 878.1820
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code OYD.