{"data":{"id":"us/21-cfr-886.4300","jurisdiction":"us","citation":"21 CFR 886.4300","heading":"Intraocular lens guide.","body":"(a) Identification. An intraocular lens guide is a device intended to be inserted into the eye during surgery to direct the insertion of an intraocular lens and be removed after insertion is completed.\n(b) Classification. Class I (general controls). Except when used as folders or injectors for soft or foldable intraocular lenses, the device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 886.9.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 886—OPHTHALMIC DEVICES","Subpart E—Surgical Devices"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"d921a8dabb28263b094696952ad6dda03e6922ac3e85cb814f73284950d9491d","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-886.4280","next":"us/21-cfr-886.4320"},"notice":"GroundRules: Original legal text. Not legal advice."}