Penny & Giles Blackwood, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Penny & Giles Blackwood, Ltd. makes
Penny & Giles Blackwood, Ltd. manufactures a goniometer and biomedical recorder system, designed for measuring joint angles and recording physiological data in clinical or research settings. The system includes hardware for angular displacement assessment and data logging, primarily used in orthopedic or rehabilitation evaluations.
The company’s products fall under FDA Class I devices and are listed via 510(k) premarket notifications. The manufacturer is based in the United States. No additional registries or classifications are specified.
Catalogue
Goniometer And Biomedical Recorder System Ref K884003
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penny & Giles Blackwood, Ltd. have in the registry?
The registry currently lists 1 device for Penny & Giles Blackwood, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penny & Giles Blackwood, Ltd.'s devices?
Among its 1 most recently registered device, Penny & Giles Blackwood, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Penny & Giles Blackwood, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Penny & Giles Blackwood, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Penny & Giles Blackwood, Ltd. in the registry?
The most recently registered devices listed for Penny & Giles Blackwood, Ltd. include GONIOMETER AND BIOMEDICAL RECORDER SYSTEM.