Home › MEDTRONIC POWERED SURGICAL SOLUTIONS › Triton®

Triton®

MEDTRONIC POWERED SURGICAL SOLUTIONS · Model ED500 · UDI-DI 00643169013148

HBE Prescription

510(k) clearances

22,777

Adverse events (3 deaths)

258

Recalls

140

Facilities

Description

DRIVER ED500 HIGH TORQUE ELECTRIC

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 key Read the docs

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.