Data / Medical devices / United States / KBD, Inc.
KBD, Inc.: FDA-registered device maker in North Las Vegas, NV, United States, 2 510(k) clearances
KBD, Inc. is registered with the FDA (registration 1022129) in North Las Vegas, NV, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 22, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1022129
- Address
- 4208 West Cheyenne Ave, Ste. 120, North Las Vegas, NV, United States, 89032
- Owner or operator
- KBD, INC. (1022129)
- Roles
- Specification developer
- First device listed
- December 17, 2008
- Registered through
- 2026
- Brand names listed
- Sperti Sunlamp Vitamin D Box
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Booth, Sun Tan | LEJ | 2 | Specification developer | accessdata.fda.gov |
| Light, Ultraviolet, Dermatological | FTC | 2 | Specification developer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Specification developer | accessdata.fda.gov |
| Sunlamp Products (Pre-Standard) | RAB | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 22, 2018 | K151721 | FIJI SUN FLUORESCENT TANNING UNIT | LEJ | Substantially Equivalent | Kdb Inc. (Dba) Sperti Sunlamp | accessdata.fda.gov |
| August 6, 1986 | K862608 | SPERTILITE PHOTOTHERAPY LAMP | FTC | Substantially Equivalent for Some Indications | Cooper-Hewitt Electric Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Light, Ultraviolet, Dermatological
- All makers of Booth, Sun Tan
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
Updated June 22, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.