Home › APEX BIOTECHNOLOGY CORP. › UASure II Blood Uric Acid Monitoring System
UASure II Blood Uric Acid Monitoring System
APEX BIOTECHNOLOGY CORP. · Model S95046 · UDI-DI 00886338000031
3
510(k) clearances
0
Adverse events
2
Recalls
5
Facilities
Description
Complete Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-04 | Visgeneer, Inc. | Due to products distributed without premarket clearance or approvals. |
| 2023-10-04 | Visgeneer, Inc. | Due to products distributed without premarket clearance or approvals. |
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.