Home › WONDFO USA CO., LTD. › PRIME SCREEN®
PRIME SCREEN®
WONDFO USA CO., LTD. · Model DCDOA-254-1BX-A · UDI-DI 00810174471045
1
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities
Description
Prime Screen®; 5- Panel T-Cup Compact; AMP,COC,mAMP,OPI,THC
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.
