Hodgkinson & Corby, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Hodgkinson & Corby, Ltd. makes
Hodgkinson & Corby, Ltd. manufactures the ORTHOTRON Muscle Stimulator MK II DC, a device designed for neuromuscular electrical stimulation to aid muscle activation and rehabilitation.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US regulatory system.
Catalogue
Orthotron Muscle Stimulator Mk Ii Dc Ref K851037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hodgkinson & Corby, Ltd. have in the registry?
The registry currently lists 1 device for Hodgkinson & Corby, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hodgkinson & Corby, Ltd.'s devices?
Among its 1 most recently registered device, Hodgkinson & Corby, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hodgkinson & Corby, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hodgkinson & Corby, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hodgkinson & Corby, Ltd. in the registry?
The most recently registered devices listed for Hodgkinson & Corby, Ltd. include ORTHOTRON MUSCLE STIMULATOR MK II DC.