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Zethon

ZETHON LIMITED · Model C07-05033 · UDI-DI 05059358038697

HBE Prescription

510(k) clearances

21,585

Adverse events (3 deaths)

258

Recalls

140

Facilities

Description

BUR - 2.38MM, FLUTED ACORN GOLD, 70MM X 5.0MM

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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Data 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.