Data / Medical devices / United States / Kings Two Dental Supply
Kings Two Dental Supply: FDA-registered device maker in City of Industry, CA, United States, 1 510(k) clearance
Kings Two Dental Supply is registered with the FDA (registration 2084813) in City of Industry, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 3, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2084813
- FEI number
- 1000124400
- Address
- 918 Canada Ct, City of Industry, CA, United States, 91748
- Owner or operator
- Kings Two Dental Supply (10039082)
- Roles
- Repackager or relabeler
- First device listed
- February 20, 2026
- Registered through
- 2026
- Brand names listed
- Nitrile Examination Powder Free
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Polymer Patient Examination Glove | LZA | 1 | Repackager or relabeler | 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 3, 1999 | K990668 | POWDER FREE BLUE NITRILE GLOVE | LZA | Substantially Equivalent | Tg Medical Sdn. Bhd. | accessdata.fda.gov |
Compare with other makers
Updated June 3, 1999. 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.