Gillette Children'S Specialty Healthcare
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- Devices
- 1
What Gillette Children'S Specialty Healthcare makes
Gillette Children’s Specialty Healthcare manufactures the CRANIOCAP, a medical device designed to support and stabilize the head and skull in pediatric patients, particularly those with craniofacial conditions or post-surgical care needs.
The CRANIOCAP is classified as a Class II device under FDA regulations and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Craniocap Ref K000861
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gillette Children'S Specialty Healthcare have in the registry?
The registry currently lists 1 device for Gillette Children'S Specialty Healthcare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gillette Children'S Specialty Healthcare's devices?
Among its 1 most recently registered device, Gillette Children'S Specialty Healthcare has devices listed in FDA 510(k) (1 device).
What risk classes do Gillette Children'S Specialty Healthcare's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gillette Children'S Specialty Healthcare's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gillette Children'S Specialty Healthcare in the registry?
The most recently registered devices listed for Gillette Children'S Specialty Healthcare include CRANIOCAP.