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Oragene Dx
DNA Genotek Inc · Model OGD-675 · UDI-DI 00627595000262
OYJ
Prescription
2
510(k) clearances
4
Adverse events
1
Recalls
16
Facilities
Description
DNA Specimen Collection, Saliva (For Assisted Collection)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-02-18 | DNA Genotek Inc. | Evaporation of stabilizing liquid reducing shelf life. |
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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.