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Drill Sleeve Guide
Ad-Tech Medical Instrument Corporation · Model DSG-6.3-090-2.4N · UDI-DI 00841823106520
10
510(k) clearances
23,371
Adverse events (3 deaths)
258
Recalls
140
Facilities
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). |
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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.