Data / Medical devices / United States / The Metz Dental Laboratory
The Metz Dental Laboratory: FDA-registered device maker in Gahanna, OH, United States, 1 510(k) clearance
The Metz Dental Laboratory is registered with the FDA (registration 3010347083) in Gahanna, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 5, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010347083
- FEI number
- 3007496177
- Address
- 104 Mill Street Suite H, Gahanna, OH, United States, 43230
- Owner or operator
- The Metz Dental Laboratory (10044377)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 3, 2013
- Registered through
- 2026
- Brand names listed
- Healthy Sleep Appliance, The Metz Appliance
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| April 5, 2013 | K123410 | HEALTHY SLEEP APPLIANCE | LRK | Substantially Equivalent | Healthy Sleep Dental Laboratory | accessdata.fda.gov |
Compare with other makers
Updated April 5, 2013. 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.