Jw North America, Inc.
United Statesfrom the FDA registration address FDA FEI 1450790
- Devices
- 75
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 75 devicesShowing 1-50 of 75
Company details
- FDA FEI number
- 1450790
- DUNS number
- 039280558
- Address
- 200 Ledgewood Place, Rockland, MA, 02370
Frequently asked questions
How many devices does JW NORTH AMERICA, INC. have in the registry?
The registry currently lists 75 devices for JW NORTH AMERICA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list JW NORTH AMERICA, INC.'s devices?
Among its 50 most recently registered devices, JW NORTH AMERICA, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do JW NORTH AMERICA, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for JW NORTH AMERICA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from JW NORTH AMERICA, INC. in the registry?
The most recently registered devices listed for JW NORTH AMERICA, INC. include COSMEDICO M 250 SE, SUPRA Q-0800PIY-L, SUPRA Q-04500SI and RADIANCE HP 600-800 GY9.5.