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Characteristics of the orthopedic DOC band™ by CRANIAL TECHNOLOGIES INC. (CTI)
The first active orthopedic band available world-wide (1986).
The dynamic head band concept is based upon the application of pressure in the relevant places.
The DOC band™ was the first to receive approval by the American Food and Drug Administration (FDA) for cranial orthoses in 1998.
In 2005 the FDA first approved the use of DOC band™ for post-surgical cases (craniostenosis).
19 medical centres all over Europe and the United States.
More than 35.000 cases de plagiocephaly and others already treated.
Applied in more than 600 post-surgery cases.
No negative short- or long-term side-effects of any kind have been observed.
Orthopedic treatment with DOC band™ is applicable in the following conditions:
- Positional plagiocephaly (front and rear)
- Positional brachycephaly
- Positional scaphocephaly
- Mixed craniofacial positional deformities
- Post-surgical treatment of classic craniosynostosis
- Post-surgical treatment of early endoscopic surgery in craniosynostosis
- Protection and remoulding in cases of parietal bone defects
The DOC band™ is formed from a lightweight anti-allegic plastic material perfectly tolerated by infants.
To be used continuously and only removed at bathtime and for neck exercises.
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