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Sign in to claim this brandQApel Medical, Inc.
US
Last updated May 23, 2026
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Catalogue (32)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Zebra | AC6074-115-20 | FDA UDI | Class II | Active |
| 6F Armadillo | FG 00735-05 | FDA UDI | Class II | Active |
| Wahoo | FG 00074 | FDA UDI | Class II | Active |
| 072 Aspiration System | FG 00806 | FDA UDI | Class II | Unknown |
| 072 Aspiration System | FG 01252 | FDA UDI | Class II | Unknown |
| Walrus | FG 00100-01 | FDA UDI | Class II | Active |
| Armadillo | FG 00464-08 | FDA UDI | Class II | Active |
| Zebra | AC7087-095-20-B | FDA UDI | Class II | Active |
| Zebra | AC7087-080-20-B | FDA UDI | Class II | Active |
| Armadillo | FG 00464-04 | FDA UDI | Class II | Active |
| Zebra | AC6074-095-20 | FDA UDI | Class II | Active |
| Armadillo | FG 00464-05 | FDA UDI | Class II | Active |
| Zebra | AC7087-105-20-B | FDA UDI | Class II | Active |
| Zebra | AC6074-105-30 | FDA UDI | Class II | Active |
| 072 Aspiration System | FG 00995 | FDA UDI | Class II | Unknown |
| Zebra | AC7087-080-20-S | FDA UDI | Class II | Active |
| Walrus | FG 00100-02 | FDA UDI | Class II | Active |
| Zebra | AC7087-105-20-S | FDA UDI | Class II | Active |
| Zebra | AC6074-080-20 | FDA UDI | Class II | Active |
| Armadillo | FG 00464-07 | FDA UDI | Class II | Active |
| Zebra | AC7087-095-20-S | FDA UDI | Class II | Active |
| Zebra | AC6074-095-30 | FDA UDI | Class II | Active |
| Zebra | AC6074-080-30 | FDA UDI | Class II | Active |
| Zebra | AC6074-115-30 | FDA UDI | Class II | Active |
| Zebra | AC6074-105-20 | FDA UDI | Class II | Active |
| Lynx Aspiration Catheter System | K254276 | FDA 510(k) | Class II | Active |
| SelectFlex Neurovascular Access System Family | K230322 | FDA 510(k) | Class II | Active |
| 072 Aspiration System | K222786 | FDA 510(k) | Class II | Active |
| 087 Balloon Guide Catheter System | K192525 | FDA 510(k) | Class II | Active |
| Neurovascular Access System Family | K240746 | FDA 510(k) | Class II | Active |
| SelectFlex 072 Neurovascular Access System | K191664 | FDA 510(k) | Class II | Active |
| SelectFlex Neurovascular Access System Family | K211893 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 26, 2025 | Z-1512-2025 | — | open, classified | Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur. |