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U.S. Department of Health and Human Services

Product Classification

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Device sunglasses (non-prescription including photosensitive)
Regulation Description Sunglasses (nonprescription).
Regulation Medical Specialty Ophthalmic
Review Panel Ophthalmic
Product CodeHQY
Premarket Review Office of Device Evaluation (ODE)
Division of Ophthalmic and Ear, Nose and Throat Devices (DOED)
Intraocular and Corneal Implants Devices Branch (ICIB)
Submission Type 510(K) Exempt
Regulation Number 886.5850
Device Class 1
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
    Note: FDA has exempted almost all class I devices (with the exception of reserved devices) from the premarket notification requirement, including those devices that were exempted by final regulation published in the Federal Registers of December 7, 1994, and January 16, 1996. It is important to confirm the exempt status and any limitations that apply with 21 CFR Parts 862-892. Limitations of device exemptions are covered under 21 CFR XXX.9, where XXX refers to Parts 862-892.
If a manufacturer's device falls into a generic category of exempted class I devices as defined in 21 CFR Parts 862-892, a premarket notification application and fda clearance is not required before marketing the device in the U.S. however, these manufacturers are required to register their establishment. Please see the Device Registration and Listing website for additional information.
Guidance Document
  • Guidance Document for Nonprescription Sunglasses; Final
Third Party Review Not Third Party Eligible
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