Home › CENTURION MEDICAL PRODUCTS CORPORATION › Centurion
Centurion
CENTURION MEDICAL PRODUCTS CORPORATION · Model IFK840 · UDI-DI 00653160056952
PRR
Prescription
0
510(k) clearances
3
Adverse events
1
Recalls
10
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-12-11 | Centurion Medical Products Corporation | Incomplete seals on the sterile package may compromise the sterility |
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.