21 CFR 876.3630
§ 876.3630 Penile rigidity implant.
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 876.3630, § 876.3630 Penile rigidity implant, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/90293
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Full text
(a) Identification. A penile rigidity implant is a device that consists of a pair of semi-rigid rods implanted in the corpora cavernosa of the penis to provide rigidity. It is intended to be used in men diagnosed as having erectile dysfunction.
(b) Classification. Class II. The special control for this device is the FDA guidance entitled “Guidance for the Content of Premarket Notifications for Penile Rigidity Implants.”
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.