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Medical Devices; Ophthalmic Devices; Classification of the Eyelid Weight

fda-device · Food and Drug Administration · Rule · Published 2014-04-21 · Effective 2014-07-21 · 79 FR 22012

Document

Document number
2014-08940
Federal Register citation
79 FR 22012
CFR reference
21 CFR 886
Type
Rule
Action
Final rule.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2014-04-21
Effective date
2014-07-21
HHS docket
Docket No. FDA-2013-N-0069

Abstract

The Food and Drug Administration (FDA or Agency) is classifying the eyelid weight into class II (special controls). The Agency is exempting the external eyelid weight from premarket notification, but continuing to require premarket notification for implantable eyelid weights in order to provide a reasonable assurance of safety and effectiveness of the device. Both external and implantable eyelid weight devices are subject to special controls. The eyelid weight may be adhered to the outer skin of the upper eyelid (external eyelid weight) or implanted into the upper eyelid (implantable eyelid weight), and is intended for the gravity assisted treatment of lagophthalmos (incomplete eyelid closure).

Source

Authoritative
Federal Register document
Machine
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