Data / Medical devices / United States / Cleartooth Electronics, Inc.
Cleartooth Electronics, Inc.: FDA-registered device maker in Boulder, CO, United States, 1 510(k) clearance
Cleartooth Electronics, Inc. is registered with the FDA (registration 3008313821) in Boulder, CO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 30, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008313821
- Address
- 106 Mineola Ct., Boulder, CO, United States, 80303
- Owner or operator
- Cleartooth Electronics, Inc. (10031351)
- Roles
- Manufacturer
- First device listed
- January 19, 2010
- Registered through
- 2026
- Brand names listed
- Cleartooth Digital X-Ray
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, X-Ray, Extraoral Source, Digital | MUH | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| December 30, 2003 | K033147 | CLEARTOOTH DIGITAL X-RAY SYSTEM | MUH | Substantially Equivalent | Cleartooth Electronics, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 30, 2003. 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.