Data / Medical devices / Germany / Natural Esthetics
Natural Esthetics: FDA-registered device maker in Fuessen Bavaria, Germany, 1 510(k) clearance
Natural Esthetics is registered with the FDA (registration 3006523393) in Fuessen Bavaria, Germany. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006523393
- Address
- Bahnhofstrasse 12, Fuessen Bavaria, Germany, 87629
- Owner or operator
- Natural Esthetics (10050358)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 8, 2015
- Registered through
- 2026
- Brand names listed
- Bioesthetic Restoration, Biorthosis, Bite, CR Record, Dental impression based on resin / plaster, Pre-Adjustment Relaxator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Mouthguard, Prescription | MQC | U | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain | NSP | N | Manufacturer | accessdata.fda.gov |
| Wax, Dental, Intraoral | EGD | 1 | 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 |
|---|---|---|---|---|---|---|
| April 11, 2014 | K134015 | M-PM-DISC | MQC | Substantially Equivalent | Merz Dental GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Wax, Dental, Intraoral
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Mouthguard, Prescription
- All makers of Restoration, Porcelain
Updated April 11, 2014. 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.