E.M. Adams
United Statesfrom the FDA registration address FDA FEI 1000114163
- Devices
- 1,606
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What E.M. Adams makes
E.M. Adams manufactures reusable limb, torso, and head restraints, as well as single-use and non-medicated surgical kits and tools. These include suture and circumcision kits, general surgical procedure kits, and forceps designed for soft-tissue manipulation or dressing utility. The company also produces single-use scissors-like and tweezers-like surgical forceps.
The portfolio includes devices classified as Class I and Class II under FDA regulations, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 1,606 devicesShowing 1-50 of 1,606
Company details
- FDA FEI number
- 1000114163
- Address
- 7496 COMMERCIAL CIRCLE, FORT PIERCE, FL, 34951
Frequently asked questions
How many devices does E.M. Adams have in the registry?
The registry currently lists 1606 devices for E.M. Adams. Devices recorded under merged duplicate company entries are counted once.
Which registries list E.M. Adams's devices?
Among its 50 most recently registered devices, E.M. Adams has devices listed in FDA GUDID (50 devices).
What risk classes do E.M. Adams's devices fall under?
Among its 50 most recently registered devices, the classes recorded for E.M. Adams's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from E.M. Adams in the registry?
The most recently registered devices listed for E.M. Adams include E.M. Adams Co, Inc. EP80201XXLPB-1, E.M Adams co, inc. EP26-0483XXLPB-1, E.M. Adams co, inc. EP28-0105SU-1 and E.M Adams co, inc. EP28-0303SB-1.