VALENCIA TECHNOLOGIES CORPORATION
FDA registration: United States Last updated 25 Oct 2026
- Devices
- 7
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
eCoin Explant Kit 1011-4262 Ref 1011-4262
eCoin External Controller Kit 1011-1752 Ref 1011-1752
eCoin External Controller Kit 1011-5436 Ref 1011-5436
eCoin Device Kit 1011-2447 Ref 1011-2447
eCoin Patient Kit 1011-1901 Ref 1011-1901
eCoin Procedural Kit 1011-2700 Ref 1011-2700
eCoin Aftercare Kit 1011-2813 Ref 1011-2813
What VALENCIA TECHNOLOGIES CORPORATION makes
Valencia Technologies Corporation manufactures implantable tibial nerve stimulation systems for incontinence control, as well as external controller kits to manage the device externally. The company also produces general surgical procedure kits containing medicated supplies and non-sterile, non-medicated wound dressing kits for post-operative care.
The portfolio includes devices classified as Class I, Class II, and Class III under FDA regulations, all listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Frequently asked questions
How many devices does VALENCIA TECHNOLOGIES CORPORATION have in the registry?
The registry currently lists 7 devices for VALENCIA TECHNOLOGIES CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list VALENCIA TECHNOLOGIES CORPORATION's devices?
Among its 7 most recently registered devices, VALENCIA TECHNOLOGIES CORPORATION has devices listed in FDA GUDID (7 devices).
What risk classes do VALENCIA TECHNOLOGIES CORPORATION's devices fall under?
Among its 7 most recently registered devices, the classes recorded for VALENCIA TECHNOLOGIES CORPORATION's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from VALENCIA TECHNOLOGIES CORPORATION in the registry?
The most recently registered devices listed for VALENCIA TECHNOLOGIES CORPORATION include eCoin Explant Kit 1011-4262, eCoin External Controller Kit 1011-1752, eCoin External Controller Kit 1011-5436 and eCoin Device Kit 1011-2447.
Information
- FDA registration
- United States
- Address
- 28464 Westinghouse Place, Valencia, CA, 91355
- FDA FEI number
- 3010878085