Home › GEROA DIAGNOSTICS SOCIEDAD LIMITADA. › GeroaDX
GeroaDX
GEROA DIAGNOSTICS SOCIEDAD LIMITADA. · Model 1 · UDI-DI 08437029987012
8
510(k) clearances
0
Adverse events
1
Recalls
10
Facilities
Description
ELISA Kit for Human Lactoferrin For In Vitro Diagnostic Use
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-03-27 | IMMUNDIAGNOSTIK, Inc | Marketed without a 510k |
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.
