StacksVerified U.S. regulatory reference

21 CFR §876.3630

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov
  1. (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.
  2. (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.”