Home › KOROS U.S.A., INC. › Elevator
Elevator
KOROS U.S.A., INC. · Model 7793-23 · UDI-DI 10840199533517
HTE
Prescription
0
510(k) clearances
137
Adverse events (1 deaths)
3
Recalls
175
Facilities
Description
Spetzer Type Elevator
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
| 2013-09-24 | SpineFrontier, Inc. | Handles and heads may not be compatible. |
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.