Devices

Device Recall LokomatSystem

Model / Serial
Software Versions: V4.30, V4.31, V4.31a, V4.31b, V4.31c, V4.32, V4.32a and V5.0x.
Product Classification
Physical Medicine Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution -- including IL, MA, MI, NY and OH.
Product Description
Hocoma Lokomat-System with Pediatric Module || Software Versions: V4.30, V4.31, V4.31a, V4.31b, V4.31c, V4.32, V4.32a, V5.0x. || Powered exercise equipment used to apply automated locomoter training for hemiplegic and paraplegic patients.
Manufacturer
Hocoma AG
1 Event
- Recall of Device Recall LokomatSystem

Manufacturer

Hocoma AG

Manufacturer Address
Hocoma AG, Florastrasse 47, Zuerich Switzerland
Manufacturer Parent Company (2017)
Hocoma Ag
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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