Silverceuticals Inc
United Statesfrom the FDA registration address FDA FEI 3025697678
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Silverceuticals Inc makes
Silverceuticals Inc manufactures non-medicated adhesive bandages designed for minor skin abrasions and cuts. Their product line includes the Naked Bandage, a simple, single-use dressing intended for basic wound coverage and protection.
The company’s adhesive bandages are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.
Catalogue
SilverCeuticals® Antimicrobial Wound Gel Ref K251929
Regimes: 510(k) Registry: 510(k)- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3025697678
- DUNS number
- 118634470
- Address
- 1396 W 200 S, Suite 2C, Lindon, UT, 84042
- [email protected]
- Phone
- 385-212-4044
Frequently asked questions
How many devices does Silverceuticals Inc have in the registry?
The registry currently lists 3 devices for Silverceuticals Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silverceuticals Inc's devices?
Among its 3 most recently registered devices, Silverceuticals Inc has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Silverceuticals Inc's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Silverceuticals Inc's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Silverceuticals Inc in the registry?
The most recently registered devices listed for Silverceuticals Inc include SilverCeuticals® Antimicrobial Wound Gel, Naked Bandage 4x12 and Naked Bandage 4x4.