Encore, Inc.
United Statesfrom the FDA registration address FDA FEI 1527982
Encore, Inc. is a medical device manufacturer, with 46 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 46
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 45
- FDA 510(k) 1
- Device classes
- FDA Class II 46
- Identifiers
- FDA FEI 1527982
- DUNS 614647725
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 46 devicesCompany details
- FDA FEI number
- 1527982
- DUNS number
- 614647725
- Address
- 6487 Parkland Drive, SARASOTA, FL, 34243
- Phone
- 800-475-3091
Frequently asked questions
How many devices does ENCORE, INC. have in the registry?
The registry currently lists 46 devices for ENCORE, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ENCORE, INC.'s devices?
Among its 46 most recently registered devices, ENCORE, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (45 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ENCORE, INC.'s devices fall under?
Among its 46 most recently registered devices, the classes recorded for ENCORE, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ENCORE, INC. in the registry?
The most recently registered devices listed for ENCORE, INC. include Encore AMERICAN CONE, Encore 20/Master, Encore VA VTU-E and Encore SILICONE RING #5.