Ophthalmic 13
- Labeling Recommendations for Hydrogen Peroxide-Based Contact Lens Care Products
- Testing and Performance Requirements for Soft Daily Wear Contact Lenses
- Patient Labeling for Laser-Assisted In Situ Keratomileusis (LASIK) Devices (DRAFT)
- 510k Exemption for Unclassified Medical Devices in Selected Product Categories
- Evaluation and Reporting of Age, Race, and Ethnicity Data in Medical Device Clinical Studies
- Procedures for Medical Devices Advisory Committee Panel Meetings
- Use of Real-World Data to Generate Evidence for Medical Device Regulatory Decisions
- Assessment of Radiofrequency-Induced Heating in Multi-Configuration Passive Medical Devices for MR Conditional Labeling
- Applying Human Factors Engineering and Usability Engineering to Medical Devices
- Implantable Minimally Invasive Glaucoma Surgical (MIGS) Devices - Testing and Clinical Requirements
- Endotoxin Testing for Single-Use Intraocular Ophthalmic Devices
- Retinal Prostheses: Clinical, Non-Clinical, and Safety Recommendations for Electrical Stimulation Devices
- Contact Lens Care Product Labeling: Warnings, Instructions and Readability Requirements