Depuy Intl., Ltd.
United KingdomFDA applicant, unverified FDA FEI 1000199976
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Depuy Intl., Ltd. makes
Depuy Intl., Ltd. manufactures dermatomes, including the DECA Dermatome, a micromotor-driven device used for precise skin grafting procedures. These tools are designed to create uniform skin slices for medical applications, such as reconstructive surgery.
The company’s dermatomes fall under Class I regulatory classification in the U.S., with relevant devices listed via 510(k) clearance through the FDA. The manufacturer operates from the United States.
Catalogue
Deca Dermatome (Micromotor System) Ref K945594
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000199976
- Address
- ST. ANTHONYS RD., LEEDS
Frequently asked questions
How many devices does Depuy Intl., Ltd. have in the registry?
The registry currently lists 1 device for Depuy Intl., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Depuy Intl., Ltd.'s devices?
Among its 1 most recently registered device, Depuy Intl., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Depuy Intl., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Depuy Intl., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Depuy Intl., Ltd. in the registry?
The most recently registered devices listed for Depuy Intl., Ltd. include DECA DERMATOME (MICROMOTOR SYSTEM).