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Sign in to claim this brandSpark Biomedical Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 7535 W Grand Pkwy S, Richmond, TX, 77407
- Website
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3017987352
- DUNS Number
- —
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sparrow Ascent Earpiece, Right | 211 | FDA UDI | Class II | Active |
| Sparrow Ascent Cable | 810-P | FDA UDI | Class II | Active |
| Sparrow Ascent 28 Piece Kit (B2B) | 11-320-K-28 | FDA UDI | Class II | Active |
| Sparrow Ascent Cable | 810 | FDA UDI | Class II | Active |
| Sparrow Ascent Earpiece, Left | 210 | FDA UDI | Class II | Active |
| Sparrow Ascent 28 Piece Kit (B2C) | 11-310-K-28 | FDA UDI | Class II | Active |
| Sparrow Ascent Kit (B2B) | 11-320-K | FDA UDI | Class II | Active |
| Sparrow Ascent Kit (B2C) | 11-310-K | FDA UDI | Class II | Active |
| Sparrow Ascent Patient Controller | 110 | FDA UDI | Class II | Active |
| Sparrow Ascent Replacement Kit | 11-110-K | FDA UDI | Class II | Active |
| Sparrow Ascent | K230796 | FDA 510(k) | Class II | Active |
| Sparrow Therapy System | K201873 | FDA 510(k) | Class II | Active |
| Sparrow Ascent | K251246 | FDA 510(k) | Class II | Active |
Related Companies
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No authorised representatives on record.
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Authorities
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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 |
|---|---|---|---|---|
| Jul 2, 2025 | Z-2287-2025 | — | open, classified | Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output. |