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Title 21

Displaying title 21, up to date as of 7/16/2026. Title 21 was last amended 7/09/2026.
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Title 21Food and DrugsPart / Section
Chapter IFood and Drug Administration, Department of Health and Human Services1 – 1299
Subchapter HMedical Devices800 – 898
Part 886Ophthalmic Devices886.1 – 886.5933
Subpart AGeneral Provisions886.1 – 886.9
§ 886.1Scope.
§ 886.3Effective dates of requirement for premarket approval.
§ 886.9Limitations of exemptions from section 510(k) of the Federal Food, Drug, and Cosmetic Act (the act).
Subpart BDiagnostic Devices886.1040 – 886.1945
Subpart C [Reserved]
Subpart DProsthetic Devices886.3100 – 886.3920
§ 886.3100Ophthalmic tantalum clip.
§ 886.3130Ophthalmic conformer.
§ 886.3200Artificial eye.
§ 886.3300Absorbable implant (scleral buckling method).
§ 886.3320Eye sphere implant.
§ 886.3340Extraocular orbital implant.
§ 886.3400Keratoprosthesis.
§ 886.3600Intraocular lens.
§ 886.3800Scleral shell.
§ 886.3920Aqueous shunt.
Subpart ESurgical Devices886.4070 – 886.4855
Subpart FTherapeutic Devices886.5100 – 886.5933