Home › Cerenovus, Inc. › CODMAN
CODMAN
Cerenovus, Inc. · Model 26-1246 · UDI-DI 20886704005145
HBE
Prescription
10
510(k) clearances
22,777
Adverse events (3 deaths)
258
Recalls
140
Facilities
Description
CODMAN Cranio-blade Disposable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
| 2026-04-30 | SURGIFY MEDICAL OY | Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). |
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.