Data / Medical devices / United States / Davis Dental Lab
Davis Dental Lab: FDA-registered device maker in Wyoming, MI, United States, 1 510(k) clearance
Davis Dental Lab is registered with the FDA (registration 3004935484) in Wyoming, MI, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 18, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004935484
- Address
- 5830 Crossroads Commerce Pkwy., Wyoming, MI, United States, 49519
- Owner or operator
- National Dentex LLC (9052467)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- February 1, 2008
- Registered through
- 2026
- Brand names listed
- DSG Relaxer, Elastic Mandibular Advancement (EMA) Appliance, PM Positioner, SomnoDent MAS, Surgical Guide, TAP Anti-snoring Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Device, Anti-Snoring | LRK | 2 | Contract manufacturer | accessdata.fda.gov |
| Device, Jaw Repositioning | LQZ | 2 | Contract manufacturer | accessdata.fda.gov |
| Mouthguard, Prescription | MQC | U | Manufacturer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| March 18, 2003 | K022627 | DSG RELAXER SPLINT | MQC | Substantially Equivalent | Sentage Corporation D/B/A/ Dental Services Group | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Anti-Snoring
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Mouthguard, Prescription
- All makers of Device, Jaw Repositioning
- All makers of Accessories, Implant, Dental, Endosseous
Updated March 18, 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.