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Prosthesis, Testicular

FDA product code FAF · Class 3 · Gastroenterology, Urology

4
Registered devices
153
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Torosa — Coloplast A/STorosa — Coloplast A/STorosa — Coloplast A/STorosa — Coloplast A/S

Recent recalls

DateFirmReason
2010-04-30Coloplast Manufacturing US, LLCOn April 22, 2010, a decision was made by Coloplast to conduct a field correction based on a report that the Saline Filled Testicular Prosthesis is considered m

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.