Hocoma

Products: rehab-exoskeleton. Risk band: Low RobotRisk index 14.5/100 (severity- and time-weighted incidents) · ranked 18 of 25 among Medical robotics companies with incidents (173 tracked).

Analyst brief

Hocoma's record in the medical-robotics category holds two entries: a 2015 report of a proximal tibia fracture in a spinal-cord-injury patient associated with robotic rehabilitation, and a 2020 FDA Class II recall of the Lokomat Pro system. The two events differ in type and severity, an injury rated 2 and a recall rated 3, showing a pattern that spans both a documented adverse event and a subsequent regulatory correction on the same product line. Hocoma's index of 14.5 ranks 18 of 25 companies in Medical robotics with incident history. The record combines an injury report with a regulator-driven recall, rather than resting on a single source type.

Risk index

14.5/100RobotRisk index

22.1/100Median index across the 25 Medical robotics companies with incident history (173 tracked, 148 with none)

18 of 25Rank in Medical robotics (of 25 with incident history)

LowRisk band

Incident timeline

Comparisons over time

Per-type breakdown

Incident type	Unique incidents	Share
recall	1	50%
injury	1	50%

Unique incident list

2 unique incidents on file for this company.

Sev	Date	Type	Location	Incident	Source
S3	08 Jun 2020	recall	—	FDA Class II recall: Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD · Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD	openFDA enforcement
S2	30 Jun 2015	injury	—	Proximal tibia fracture in a patient with incomplete spinal cord injury associated with robotic treadmill training · 1 patient	nature.com