Home › PERSONAL MEDICAL CORP. › C3
C3
PERSONAL MEDICAL CORP. · Model Male Continence Device · UDI-DI 08519520073347
FHA
Prescription
10
510(k) clearances
26
Adverse events
1
Recalls
70
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-16 | Aesculap Implant Systems LLC | The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.