Prosthesis, Penile
FDA product code FAE · Class 2 · 16 devices · 693 reports · 0 devices named in recalls
- TACTRA 720081-01Boston Scientific Corporation · PROSTHESIS, PENILE150 reports
- Spectra 720074-02American Medical Systems, Inc. · Prosthesis, Penile97 reports
- Genesis 91-9511SCColoplast A/S · PROSTHESIS, PENILE85 reports
- TACTRA 720080-01Boston Scientific Corporation · PROSTHESIS, PENILE61 reports
- Genesis 91-9509SCColoplast A/S · PROSTHESIS, PENILE49 reports
- TACTRA 720082-01Boston Scientific Corporation · PROSTHESIS, PENILE49 reports
- Spectra 720074-03American Medical Systems, Inc. · Prosthesis, Penile47 reports
- Spectra 720054-02American Medical Systems, Inc. · Prosthesis, Penile44 reports
- Genesis 91-9513SCColoplast A/S · PROSTHESIS, PENILE28 reports
- Spectra 720056-03American Medical Systems, Inc. · Prosthesis, Penile25 reports
- Spectra 720074-01American Medical Systems, Inc. · Prosthesis, Penile22 reports
- Spectra 720054-01American Medical Systems, Inc. · Prosthesis, Penile19 reports
- Spectra 720056-02American Medical Systems, Inc. · Prosthesis, Penile11 reports
- Spectra 720054-03American Medical Systems, Inc. · Prosthesis, Penile4 reports
- Spectra 720056-01American Medical Systems, Inc. · Prosthesis, Penile1 report
- Spectra RTE Kit 720170-01American Medical Systems, Inc. · Prosthesis, Penile1 report