Medical Devices; Ophthalmic Devices; Classification of Nasolacrimal Compression Device. Final order
Related Experiment Video
Updated: Mar 19, 2026

07:30
Transcanalicular Diode Laser-assisted Dacryocystorhinostomy for the Treatment of Primary Acquired Nasolacrimal Duct Obstruction
Published on: October 13, 2017
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Federal Register
|June 15, 2016
Abstract:
The Food and Drug Administration (FDA) is classifying the nasolacrimal compression device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and effectiveness of the device.
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